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123lol456 123lol456
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Question 1.

Select an appropriate synthetic route of the compound shown starting with 4-methyl-2-pentanol.




▸ 1. TsCl, pyr; 2. KOtBu; 3. HBr/ROOR; 4.


▸ 1. TsCl, pyr; 2. KOtBu; 3. HCl/ROOR; 4.


▸ 1. TsCl, pyr; 2. KOtBu; 3. HBr/ROOR; 4.


▸ 1. TsCl, pyr; 2. KOtBu; 3. HBr; 4. H3O+; 5.


▸ 1. TsCl, pyr; 2. KOtBu; 3. HBr/ROOR; 4.

Question 2.

Starting with a primary alkyl bromide, which of the choices given results in an overall increase in the length of the carbon skeleton by one carbon?

▸ substitute bromide with acetylide, then cleave the triple bond

▸ substitute bromide with methoxide

▸ eliminate hydrogen bromide to produce an alkene

▸ substitute bromide with acetylide, then reduce the alkyne to an alkene
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Organic Chemistry

Organic Chemistry


Edition: 4th
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kaitmawkaitmaw
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123lol456 Author
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2 years ago
Smart ... Thanks!
ouasfoudgewu
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Yesterday
Just got PERFECT on my quiz
Transonic
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2 hours ago
Thanks for your help!!
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