Chapter 3.7, Problem 26P

(a)

Interpretation Introduction

Interpretation:

The systematic name and common name of the given amine compound has to be written and whether it is primary or secondary or tertiary amine has to be ascertained.

Concept introduction:

The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).  IUPAC name consists of three parts in major namely Prefix, suffix and root word.

The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments.

For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon.  For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.

Prefix: Represents the substituent present in the molecule and its position in the root name.

Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, amines. alcohol etc. For example alkynes molecules, suffix will be ‘yne’, if amine presence of given molecules, suffix will be “ine”.

Root word represents the longest continuous carbon skeleton of the organic molecule.

(b)

Interpretation Introduction

Interpretation:

The systematic name and common name of the given amine compound has to be written and whether it is primary or secondary or tertiary amine has to be ascertained.

Concept introduction:

The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry).  IUPAC name consists of three parts in major namely Prefix, suffix and root word.

The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.

Prefix: Represents the substituent present in the molecule and its position in the root name.

Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, amines. alcohol etc.  For example alkynes molecules, suffix will be ‘yne’, if amine presence of given molecules, suffix will be “ine”.

Root word represents the longest continuous carbon skeleton of the organic molecule.

(c)

Interpretation Introduction

Interpretation:

The systematic name and common name of the given amine compound has to be written and whether it is primary or secondary or tertiary amine has to be ascertained.

Concept introduction:

The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix, suffix and root word.

The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.

Prefix: Represents the substituent present in the molecule and its position in the root name.

Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, amines. alcohol etc. For example alkynes molecules, suffix will be ‘yne’, if amine presence of given molecules, suffix will be “ine”.

Root word represents the longest continuous carbon skeleton of the organic molecule.

(d)

Interpretation Introduction

Interpretation:

The systematic name and common name of the given amine compound has to be written and whether it is primary or secondary or tertiary amine has to be ascertained.

Concept introduction:

The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix, suffix and root word.

The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.

Prefix: Represents the substituent present in the molecule and its position in the root name.

Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, amines. alcohol etc. For example alkynes molecules, suffix will be ‘yne’, if alcohol presence of given molecules, suffix will be “ol”.

Root word represents the longest continuous carbon skeleton of the organic molecule.

(e)

Interpretation Introduction

Interpretation:

The systematic name and common name of the given amine compound has to be written and whether it is primary or secondary or tertiary amine has to be ascertained.

Concept introduction:

The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix, suffix and root word.

The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.

Prefix: Represents the substituent present in the molecule and its position in the root name.

Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, amines. alcohol etc. For example alkynes molecules, suffix will be ‘yne’, if alcohol presence of given molecules, suffix will be “ol”.

Root word represents the longest continuous carbon skeleton of the organic molecule.

(f)

Interpretation Introduction

Interpretation:

The systematic name and common name of the given amine compound has to be written and whether it is primary or secondary or tertiary amine has to be ascertained.

Concept introduction:

The many of organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix, suffix and root word.

The bond-line structure the carbon atoms and the hydrogen atoms which are attached to that carbon atom are not to show, rather the bonds in between carbon atoms and to the hetero atoms are drawn as line segments. For acyclic, linear carbon chains it draws as in a zig-zag fashion and for cyclic chains of carbon it draws as a cyclic polygon. For representing a heteroatom attached to the carbon, use a line segment and label the heteroatom at the end of their line segment.

Prefix: Represents the substituent present in the molecule and its position in the root name.

Suffix: Denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, amines. alcohol etc. For example alkynes molecules, suffix will be ‘yne’, if alcohol presence of given molecules, suffix will be “ol”.

Root word represents the longest continuous carbon skeleton of the organic molecule.