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Hatshy [7]
3 years ago
7

Compounds X and Y are both C6H13Cl compounds formed in the radical chlorination of 3-methylpentane. Both X and Y undergo base-pr

omoted E2 elimination to give a mixture of alkenes.In water X and Y each react to form a mixture of substitution and elimination products; however, X reacts much faster than does Y.What is the structure of Y?

Chemistry
1 answer:
zubka84 [21]3 years ago
6 0

Answer:

Y is a 3-chloro-3-methylpentane.

The structure is shown in the figure attached.

Explanation:

The radical chlorination of 3-methylpentane can lead to a tertiary substituted carbon (Y) and to a secondary one (X).

The E2 elimination mechanism, as shown in the figure, will happen with a simulyaneous attack from the base and elimination of the chlorine. This means that primary and secondary substracts undergo the E2 mechanism faster than tertiary substracts.

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grin007 [14]

Answer:

<h3>The answer is 3.0 g/mL</h3>

Explanation:

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density =  \frac{mass}{volume} \\

From the question

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We have

density =  \frac{15}{5}  \\

We have the final answer as

<h3>3.0 g/mL</h3>

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3 years ago
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sveta [45]

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