a)
Interpretation:
How to carry out the transformation shown is to be stated.
Concept introduction:
The double bonds in the side chain can be reduced without affecting those in the
To state:
How to carry out the transformation shown.
b)
Interpretation:
How to carry out the transformation shown is to be stated.
Concept introduction:
The carboxylic acid or ester or the carbonyl group in
To state:
How to carry out the transformation shown.
c)
Interpretation:
How to carry out the transformation shown is to be stated.
Concept introduction:
The carboxylic acid or ester or the carbonyl group in aldehydes and ketones can be reduced without affecting the double bonds in the side chain and in the aromatic ring using LiAlH4 in ether. The alcohol can be converted in to a bromide by treating with PBr3. The bromo compound when treated with NaSH will yield the thiol required,
To state:
How to carry out the transformation shown.
Trending nowThis is a popular solution!
Chapter 17 Solutions
ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<
- Propose a possible reaction mechanism for the following transformation. Draw out the steps with the correct reaction arrows.arrow_forwardAldehydes and ketones react with thiols to yield thioacetals just as they react with alcohols to yield acetals. Predict the product of the following reaction, and propose a mechanism:arrow_forward