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Explain why that is the answer please. Provided the possible synthons for each b

ID: 779434 • Letter: E

Question

Explain why that is the answer please.

Provided the possible synthons for each bond formation, which bond is most likely involved in the synthesis of the alkyne shown, and why? 2 because an sp3 hybridized carbanion is a more stable synthon than an sp hybridized carbanion synthon 2 because an sp hybridized carbanion is a more stable synthon than an sp3 hybridized carbanion synthon 1 because an sp3 hybridized carbanion is a more stable synthon than an sp hybridized carbanion synthon 1 because an sp hybridized carbanion is a more stable synthon than an sp3 hybridized carbanion synthon Provide a correct name for the molecule shown. (3E, 4R)-3,4-dimethylhept-2-en-6-yne (4S)-5-ethynyl-3,4-dimethylhex-2-ene (3R, 4Z)-3,4-dimethylhept-4-en-1-yne (3S, 4E)-1-ethynyl-1,2-dimethylbut-1-yne

Explanation / Answer

4) Answer is ( A) because sp3 hybridised un substituted carbanion is very very stable as compared to a sp hybridised carbabion. 5) Answer is (c) (3R,4Z)-3,4-dimethylhept-4-en-1-yne.

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