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Which of the amines listed next is resolved into enantiomers? In each case, explain why

Chapter 19, Problem PROBLEM 19-4

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QUESTION:

Which of the amines listed next is resolved into enantiomers? In each case, explain why interconversion of the enantiomers does or does not take place.

(a) cis-2-methylcyclohexanamine

(b) N-ethyl-N-methylcyclohexanamine

(c) N-methylaziridine

(d) ethylmethylanilinium iodide

(e) methylethylpropylisopropylammonium iodide

Questions & Answers

QUESTION:

Which of the amines listed next is resolved into enantiomers? In each case, explain why interconversion of the enantiomers does or does not take place.

(a) cis-2-methylcyclohexanamine

(b) N-ethyl-N-methylcyclohexanamine

(c) N-methylaziridine

(d) ethylmethylanilinium iodide

(e) methylethylpropylisopropylammonium iodide

ANSWER:

Step 1 of 5

(a)

This compound is resolvable into enantiomers. The group attached to starred carbon are different. Hence it is chiral. Thus it can be resolvable into enantiomers.

                                                           

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