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Questions are a continuation of questions 2,3. Thank you for you help! I really need help...

Question

Questions are a continuation of questions 2,3. Thank you for you help! I really need help...

Questions are a continuation of questions 2,3. Thank you for you help! I really need help with just 3&4.

3.Suppose you wish to perform the reation you wrote in problem 2 on the other -OH group.How might you prepare the molecule in order to do so? Suggest appropiate reagents and draw your expected products.

4. Suppose after your preparation performed in problem 3, the molecule reacts very slowly with HBr. How could you prepare the -OH group you want to see react so that it will be more reactive with HBr? in problem 2 on the other -OH group. How might you prepare the molecule in order to do so? Suggest appropiate reagents and draw you expected products.

Reactions Involving Carbon-Oxygen Bonds 1) Show the mechanism for the following reaction of an epoxide with water (and dilute acid). Indicate stereochemistry H, H20 2) The product is a diol. If you take the product and add HBr, which -OH group will react, and what will be your new product? Justify your reasoning.

Reactions Involving Carbon-Oxygen Bonds 1) Show the mechanism for the following reaction of an epoxide with water (and dilute acid). Indicate stereochemistry H, H20 2) The product is a diol. If you take the product and add HBr, which -OH group will react, and what will be your new product? Justify your reasoning.

Answers

It can give more stable carbo cation H+, H20 он он HBr он Br


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