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When an alkyne such as 2,3-dichloropentane is treated with excess sodium amide, a two-step elimination reaction will happen. The reaction would then yield the final product in the form of 2-pentyne. Its structure is shown in the attached image.
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Answer:
2-methylene propylbenzene
Explanation:
The Wittig Reaction is a reaction that converts aldehydes and ketones into alkenes through reaction with a phosphorus ylide.
The ketone in this case is 1-phenylpropan-1-one. The provided phosphonium ylide is shown in the image attached. The reaction involves;
i) alkylation
ii) addition
The product of the major organic product of the reaction is 2-methylene propylbenzene.
Explanation:
Electronic configuration of Nitrogen -
₇N = 1s² 2s² 2p³