b. A third alcohol product is formed under these conditions that is not one of the two possible products discussed in part a. This third product does not contain a cyclopentane ring. Draw this product.

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Chapter1: Chemical Foundations
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please answer parts b and c only
b. A third alcohol product is formed under these conditions that is not one of the
two possible products discussed in part a. This third product does not contain
a cyclopentane ring. Draw this product.
Page 1 of 2
c. Suppose you wanted to form the secondary alcohol described in part a. and
did not want to form any of the other product described in part b. Draw a full
reaction scheme including starting material(s), reagent(s), and product(s) for
the reaction that would accomplish this (a reaction mechanism is not
necessary).
Transcribed Image Text:b. A third alcohol product is formed under these conditions that is not one of the two possible products discussed in part a. This third product does not contain a cyclopentane ring. Draw this product. Page 1 of 2 c. Suppose you wanted to form the secondary alcohol described in part a. and did not want to form any of the other product described in part b. Draw a full reaction scheme including starting material(s), reagent(s), and product(s) for the reaction that would accomplish this (a reaction mechanism is not necessary).
1. Consider the reaction scheme below
Dilute Acid (H3O*)
a. Draw two different possible arrow pushing mechanisms for the hydration of
this alkene according to the reaction conditions shown above to yield either a
secondary or a primary alcohol as products (one mechanism for each potential
product). Explain which product would form preferentially over the other, and
specifically label an intermediate that can explain the observed
regioselectivity and provide a brief explanation for your choice. Note: do not
consider any potential rearrangements for your answer in part a.
Transcribed Image Text:1. Consider the reaction scheme below Dilute Acid (H3O*) a. Draw two different possible arrow pushing mechanisms for the hydration of this alkene according to the reaction conditions shown above to yield either a secondary or a primary alcohol as products (one mechanism for each potential product). Explain which product would form preferentially over the other, and specifically label an intermediate that can explain the observed regioselectivity and provide a brief explanation for your choice. Note: do not consider any potential rearrangements for your answer in part a.
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