Draw the major organic product for the reaction of 1-phenylpropan-1-one with the provided phosphonium ylide in part 1. In part 2 answer the question about the transformation.

The product formed from this Wittig reaction with phosphonium ylide is a phenylallyl compound, 2-methylene propylbenzene. Structure and reaction synthesis is attached in file.

Part 2

The types of transformation involved are:

alkylation (as there is a transfer of alkyl group)
addition (reaction of ylide)

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Answer:

2-methylene propylbenzene (major product)

Explanation:

This reaction yields olefins and organophosphorus compound and is also known as wittig olefination. The reactants fits the category of a ketone (1-phenylpropan-1-one) and a Wittig reagent (phosphonium ylide).

Part 1: Answer in the fig. Below.

1-phenylpropan-1-one + phosphonium ylide ➡ phenylallyl compound + 2-methylene propylbenzene (major product)

Part 2.

Classical mechanisms that happened during its transformation are thus;

• nucleophilic addition

• Elimination

• cycloaddition

• [2+2]/retro-[2+2] mechanism.