For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names. Concept Introduction: If , and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively. There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given. The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes . If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent. If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result. If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

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Question

Chapter 22.2, Problem 2PTS

(a)

Interpretation Introduction

Interpretation:

For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(b)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(c)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(d)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(e)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

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19.78 Write the products of the following sequences of reactions. Refer to your reaction road- maps to see how the combined reactions allow you to "navigate" between the different functional groups. Note that you will need your old Chapters 6-11 and Chapters 15-18 roadmaps along with your new Chapter 19 roadmap for these. (a) 1. BHS 2. H₂O₂ 3. H₂CrO4 4. SOCI₂ (b) 1. Cl₂/hv 2. KOLBU 3. H₂O, catalytic H₂SO4 4. H₂CrO4 Reaction Roadmap An alkene 5. EtOH 6.0.5 Equiv. NaOEt/EtOH 7. Mild H₂O An alkane 1.0 2. (CH3)₂S 3. H₂CrO (d) (c) 4. Excess EtOH, catalytic H₂SO OH 4. Mild H₂O* 5.0.5 Equiv. NaOEt/EtOH An alkene 6. Mild H₂O* A carboxylic acid 7. Mild H₂O* 1. SOC₁₂ 2. EtOH 3.0.5 Equiv. NaOEt/E:OH 5.1.0 Equiv. NaOEt 6. NH₂ (e) 1. 0.5 Equiv. NaOEt/EtOH 2. Mild H₂O* Br (f) i H An aldehyde 1. Catalytic NaOE/EtOH 2. H₂O*, heat 3. (CH,CH₂)₂Culi 4. Mild H₂O* 5.1.0 Equiv. LDA Br An ester 4. NaOH, H₂O 5. Mild H₂O* 6. Heat 7. MgBr 8. Mild H₂O* 7. Mild H₂O+

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Answer 2

Question

Chapter 22.2, Problem 2PTS

(a)

Interpretation Introduction

Interpretation:

For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(b)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(c)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(d)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(e)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

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Answer 3

Question

Chapter 22.2, Problem 2PTS

(a)

Interpretation Introduction

Interpretation:

For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(b)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(c)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(d)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(e)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

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Answer 4

Question

Chapter 22.2, Problem 2PTS

(a)

Interpretation Introduction

Interpretation:

For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(b)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(c)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(d)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(e)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

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Answer 5

Chapter 22.2, Problem 2PTS

(a)

Interpretation Introduction

Interpretation:

For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(b)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(c)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(d)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

(e)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

Answer 6

Chapter 22.2, Problem 2PTS

(a)

Interpretation Introduction

Interpretation:

For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

Answer 7

Chapter 22.2, Problem 2PTS

(a)

Interpretation Introduction

Interpretation:

For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

Answer 8

(b)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

Answer 9

(b)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

Answer 10

(c)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

Answer 11

(c)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

Answer 12

(d)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

Answer 13

(d)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

Answer 14

(e)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

Answer 15

(e)

Interpretation Introduction

Interpretation: For a given set of nitrogen containing compounds, the structures have to be drawn using their general or IUPAC names.

Concept Introduction: If, and groups are attached to the parent carbon, they are called primary, secondary and tertiary amines respectively.

There are two ways followed to name the compound. First one is the method of giving general name in which name of the alkyl group followed by amine name is given. Second one is the method giving IUPAC name in which name of the alkane group followed by amine name is given.

The length of the chain which is having more number of carbon atoms is selected as the parent or main chain. Other chains are considered as substituents to the main chain. Position of the substituents should be included in the name. If one, two, three, four, five, six, etc carbons are activating as the main chain in IUPAC system, then the name of the compound comes as methane, ethane, propane, butane, pentane, hexane, etc. which are the name of alkanes. If one, two, three, four, five, six, etc carbons are activating as the main chain in general name method, then the name of the compound comes as methyl, ethyl, propyl, butyl, pentyl, hexyl, etc. which are the name of alkyl groups. If substituent groups are attached to nitrogen atom as in the case of tertiary or secondary amines, the name is given as N-alkyl name of the substituent.

If any configuration is present in the compound, that should be assigned to it while writing the name. If the compound contains heavier groups on the same side, it gets (Z)-configuration. If they are on the opposite directions, (E)-configurations result.

If a carbon has four different groups attached to it, that carbon shows a chirality nature. If that chiral carbon rotates the plane polarized light into a clockwise direction, it gets (R)-isomer. If that carbon rotates the plane polarized light into a counter-clockwise direction, it gets (S)-isomer.

Answer 16

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Answer 17

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Answer 18

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Answer 19

Ch. 22.2 - Prob. 1LTS Ch. 22.2 - Prob. 1PTS Ch. 22.2 - Prob. 2PTS Ch. 22.2 - Prob. 3ATS Ch. 22.3 - Prob. 4CC Ch. 22.3 - Prob. 5CC Ch. 22.3 - Prob. 6CC Ch. 22.3 - Prob. 7CC Ch. 22.3 - Prob. 8CC Ch. 22.3 - Prob. 9CC

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Chapter 22 Solutions