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sladkih [1.3K]
2 years ago
14

Choose the best option for the precursor to the tosylate intermediate Design a synthesis of cis-2-methylcyclopentyl acetate from

trans-2-methylcyclopentanol.
Chemistry
1 answer:
kumpel [21]2 years ago
8 0

Answer:

To synthesize cis-2-methylcyclopentyl from methycyclopentanol, you need to replace the acetate hydroxyl group with acetate by inverting the configuration.  

Explanation:

To understand the process, you need to understand the nucleophilic mechanism taking place in the process. This is the first stage of the process. Hydroxide is a poor leaving group, to it must be converted to a good leaving group. To effect the change, it is necessary to use p-toluenesuphate.

p-toluenesuphate is favored because this can be prepared by a reaction that alters none of the bonds attached to the stereogenic center.

The reaction of p-toluensulfonate with potassium acetate in acetic acid effects the conversion to give the final product: cis-2-methylcyclopentyl.  

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2 years ago
Zn +
saul85 [17]

Answer:

1. Theoretical yield = 2.03g

2. Actual yield 1.89g

Explanation:

Let us write a balanced equation. This is illustrated below:

Zn + 2HCI —> ZnCl2 + H2

Molar Mass of HCl = 1 +35.5 = 36.5g/mol

Mass of HCl from the balanced equation = 2 x 36.5 = 73g

Molar Mass of H2 = 2x1 = 2g/mol

1. From the equation,

73g of HCl produced 2g of H2.

Therefore, 74g of HCl will produce = (74 x 2)/73 = 2.03g

Therefore, theoretical yield = 2.03g

2. %yield = 93%

Theoretical yield = 2.03g

Actual yield =?

%yield = Actual yield /Theoretical yield x100

Actual yield = %yield x theoretical yield

Actual yield = 93% x 2.03 = (93/100)x2.03 = 1.89g

Actual yield =1.89g

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Answer:

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