IUPAC name of the given compound has to be chosen from the given options. Concept Introduction: IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine. Longest carbon chain has to be identified that is attached to nitrogen atom. Suffix “-e” in name of the parent chain alkane is replaced by “-amine”. Numbering of the carbon chain is done from the end that is near the nitrogen atom. Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name. In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name. If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N -substituted primary amines. Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

Question

Draw the major substitution products you would expect for the reaction shown below. If substitution would not occur at a significant rate under these conditions, check the box underneath the drawing area instead. Be sure you use wedge and dash bonds where necessary, for example to distinguish between major products. Note for advanced students: you can assume that the reaction mixture is heated mildly, somewhat above room temperature, but strong heat or reflux is not used. Cl Substitution will not occur at a significant rate. Explanation Check :☐ O-CH + Х Click and drag to start drawing a structure.

Answer 1

Question

Chapter 6.3, Problem 3QQ

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be chosen from the given options.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

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Draw the major substitution products you would expect for the reaction shown below. If substitution would not occur at a significant rate under these conditions, check the box underneath the drawing area instead. Be sure you use wedge and dash bonds where necessary, for example to distinguish between major products. Note for advanced students: you can assume that the reaction mixture is heated mildly, somewhat above room temperature, but strong heat or reflux is not used. Cl Substitution will not occur at a significant rate. Explanation Check :☐ O-CH + Х Click and drag to start drawing a structure.

Draw the major substitution products you would expect for the reaction shown below. If substitution would not occur at a significant rate under these conditions, check the box underneath the drawing area instead. Be sure you use wedge and dash bonds where necessary, for example to distinguish between major products. Note for advanced students: you can assume that the reaction mixture is heated mildly, somewhat above room temperature, but strong heat or reflux is not used. Cl C O Substitution will not occur at a significant rate. Explanation Check + O-CH3 Х Click and drag to start drawing a structure.

✓ aw the major substitution products you would expect for the reaction shown below. If substitution would not occur at a significant rate under these conditions, check the box underneath the drawing area instead. Be sure you use wedge and dash bonds where necessary, for example to distinguish between major products. Note for advanced students: you can assume that the reaction mixture is heated mildly, somewhat above room temperature, but strong heat or reflux is not used. C Cl HO–CH O Substitution will not occur at a significant rate. Explanation Check -3 ☐ : + D Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Ce