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beks73 [17]
3 years ago
11

When 3-iodo-3-ethylpentane is treated with sodium methoxide in methanol, the major organic product is an ______ that is generate

d through an ______ mechanism.
A) ether, SN1
B) ether, SN2
C) ether, E1
D) alkene, E2
E) alkene, E1
Chemistry
1 answer:
Makovka662 [10]3 years ago
8 0

Answer:

E

Explanation:

The alkyl halide is a tertiary alkyl halide and the methoxide base is a strong base. Owing to steric effects, tertiary alkyl halides often undergo elimination instead of substitution reaction with strong bases. The elimination occurs via an E1 mechanism because the tertiary carbocation formed is stable.

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3 years ago
Okay im clueless and over thinking this question can someone please help me out
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The answer should be C

The reason for this is because:

There are 2 "I" on the right side of the equation but only 1 on the left. This means you need to add a 2 on the "KI" to get two "I".

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Marianna [84]

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