Concept explainers
(a)
Interpretation:
Structural formula for N,N-diethylpropanamide has to be drawn.
Concept Introduction:
Structure of the amide can be drawn from the IUPAC name. In the IUPAC name, the parent chain of carbon atom can be identified and then the substituents present in it can also be identified. With this information, the structure for the given compound can be drawn. In an amide the counting has to be always from the carbonyl carbon that is given the number 1.
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- Expanded structural formula
- Condensed structural formula
- Skeletal structural formula
- Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
(a)
Answer to Problem 6.114EP
The structural formula for N,N-diethylpropanamide is,
Explanation of Solution
The given name of the compound is N,N-diethylpropanamide. From the name it is understood that the parent carbon chain is propane and it contains three carbon atoms. The parent chain can be drawn as shown below,
As the given compound is an amide, one of the carbon atoms has to be carbonyl group and a nitrogen atom has to be attached to the carbonyl carbon atom.
The substituents present in the given name are two ethyl groups on the nitrogen atom. This gives the structure of the given compound as shown below,
Structural formula for the given N,N-diethylpropanamide is drawn.
(b)
Interpretation:
Structural formula for
Concept Introduction:
Structure of the amide can be drawn from the IUPAC name. In the IUPAC name, the parent chain of carbon atom can be identified and then the substituents present in it can also be identified. With these information, the structure for the given compound can be drawn. In an amide the counting has to be always from the carbonyl carbon that is given the number 1.
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- Expanded structural formula
- Condensed structural formula
- Skeletal structural formula
- Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
(b)
Answer to Problem 6.114EP
The structural formula for
Explanation of Solution
The given name of the compound is
As the given compound is an amide, one of the carbon atom has to be carbonyl group and a nitrogen atom has to be attached to the carbonyl carbon atom.
The substituent present in the given name is a methyl groups on the beta carbon atom. This gives the structure of the given compound as shown below,
Structural formula for the given
(c)
Interpretation:
Structural formula for N-methylbenzamide has to be drawn.
Concept Introduction:
Structure of the amide can be drawn from the IUPAC name. In the IUPAC name, the parent chain of carbon atom can be identified and then the substituents present in it can also be identified. With these information, the structure for the given compound can be drawn. In an amide the counting has to be always from the carbonyl carbon that is given the number 1.
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- Expanded structural formula
- Condensed structural formula
- Skeletal structural formula
- Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
(c)
Answer to Problem 6.114EP
The structural formula for N-methylbenzamide is,
Explanation of Solution
The given name of the compound is N-methylbenzamide. From the name it is understood that the parent carbon chain is benzene and it contains six carbon atoms. The parent chain can be drawn as shown below,
The name itself says that an amide group is attached to a benzene ring. On the nitrogen atom of the amide group, a methyl group is present as substituent.
Structural formula for the given N-methylbenzamide is drawn.
(d)
Interpretation:
Structural formula for
Concept Introduction:
Structure of the amide can be drawn from the IUPAC name. In the IUPAC name, the parent chain of carbon atom can be identified and then the substituents present in it can also be identified. With these information, the structure for the given compound can be drawn. In an amide the counting has to be always from the carbonyl carbon that is given the number 1.
The structural representation of organic compound can be done in 2D and 3D. In two-dimensional representation, there are four types of representation in which an organic compound can be drawn. They are,
- Expanded structural formula
- Condensed structural formula
- Skeletal structural formula
- Line-angle structural formula
Structural formula which shows all the atoms in a molecule along with all the bonds that is connecting the atoms present in the molecule is known as Expanded structural formula.
Structural formula in which grouping of atoms are done and in which the central atoms along with the other atoms are connected to them are treated as group is known as Condensed structural formula.
Structural formula that shows the bonding between carbon atoms alone in the molecule ignoring the hydrogen atoms being shown explicitly is known as Skeletal structural formula.
Structural formula where a line represent carbon‑carbon bond and the carbon atom is considered to be present in each point and the end of lines is known as Line-angle structural formula.
(d)
Answer to Problem 6.114EP
The structural formula for
Explanation of Solution
The given name of the compound is
As the given compound is an amide, one of the carbon atom has to be carbonyl group and a nitrogen atom has to be attached to the carbonyl carbon atom.
The substituents present in the given name are three methyl groups. Out of this two on beta carbon atom and one on nitrogen atom. This gives the structure of the given compound as shown below,
Structural formula for the given
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Chapter 6 Solutions
EBK ORGANIC AND BIOLOGICAL CHEMISTRY
- Michael Reactions 19.52 Draw the products from the following Michael addition reactions. 1. H&C CH (a) i 2. H₂O* (b) OEt (c) EtO H₂NEt (d) ΕΙΟ + 1. NaOEt 2. H₂O' H H 1. NaOEt 2. H₂O*arrow_forwardRank the labeled protons (Ha-Hd) in order of increasing acidity, starting with the least acidic. НОН НЬ OHd Онсarrow_forwardCan the target compound at right be efficiently synthesized in good yield from the unsubstituted benzene at left? ? starting material target If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area. Be sure you follow the standard ALEKS rules for submitting syntheses. + More... Note for advanced students: you may assume that you are using a large excess of benzene as your starting material. C :0 T Add/Remove step Garrow_forward
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- Which one of the following atoms should have the largest electron affinity? a) b) c) d) 으으 e) 1s² 2s² 2p6 3s¹ 1s² 2s² 2p5 1s² 2s² 2p 3s² 3p² 1s² 2s 2p 3s² 3p6 4s2 3ds 1s² 2s² 2p6arrow_forwardAll of the following are allowed energy levels except _. a) 3f b) 1s c) 3d d) 5p e) 6sarrow_forwardA student wants to make the following product in good yield from a single transformation step, starting from benzene. Add any organic reagents the student is missing on the left-hand side of the arrow, and any addition reagents that are necessary above or below the arrow. If this product can't be made in good yield with a single transformation step, check the box below the drawing area. Note for advanced students: you may assume that an excess of benzene is used as part of the reaction conditions. : ☐ + I X This product can't be made in a single transformation step.arrow_forward
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