A chiral amine A having the R configuration undergoes Hofmann elimination to form an alkene B as the major product. B is oxidatively cleaved with ozone, followed by CH3SCH3, to form CH2═O and CH3CH2CH2CHO. What are the structures of A and B? Indicate stereochemistry where appropriate.

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Answer:

The Structure of "B" is alkene.

Explanation:

The compound "A" having R- configuration  and undergoes Hofmann elimination to form an alkene.

The compound "B" on oxidatively cleaving with ozone followed by dimethyl sulfide forms [tex]CH_{2}=S[/tex] and [tex]CH_{3}CH_{2}CH_{2}CHO[/tex]

The structure of "A" and"B" is as follows.

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