Question

Which of the following substituents will have a greater influence on shown below? the s x- Me Me
Consider the alkene below. If it has a pre-existing chiral center at either A, B or C (not all three would be substituted at the same time), which position (A,B or C) would you expect to have the greatest influence on the stereochemical outcome of the reaction to sa
QUESTION 3 When two achiral reagents are reacted what is the outcome? Unequal mixture of stereoisomers Well distributed mixture of stereoisomers Racial mixture of stereoisomers Equal mixture of stereoisomers QUESTION 4 If a pre-existing chiral center is present, it will not dictate the ratio of product stereoisomers True False
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Answer #1

Question 1

second option will be correct. It is because epoxidation normally chooses the side with less steric hindrance. So X = tertiary butyl group have highest steric hindrance in the given options. So apoxidation happens in the opposite direction of X. So given steriochemical outcome of the product is obtained more likely when X= tertiary butyl group.

Question 2

Third option will be correct. Substitution at A will give more steric hindrance for apoxidation compared to substitution at other two positions B and C. So substitution at A will result in the given product.

Question 3

When the two reagents are achiral then the product will be racemic mixture. That is 50-50 mixture of two enantiomers. That means racial mixture of stereoisomers.

Question 4

True

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