We are asked to provide an equation for the transformation of 2-phenylethanoic acid to 2-phenylethanol. This type of a reaction is converting a carboxylic acid to an alcohol, which is classified as a reduction reaction since we are decreasing the number of bonds to oxygen in the molecule. In order to reduce a carbonyl to an alcohol, we need a source of hydride, H⁻. Reducing the carboxylic acid once will convert it to the aldehyde. However, we need to reduce the functional group all the way down to an alcohol, which is another reduction step after aldehyde formation. Therefore, the hydride source of choice is lithium aluminum hydride, LiAlH₄.
A reaction scheme is provided to show the reaction of the reduction of carboxylic acid to alcohol. The first step is addition of lithium aluminum hydride which does the reduction, and the second step is a work-up of acid which protonates the alcohol to get the final product.
D is true because NO2 is a catalyst, and a catalyst is a compound which makes a reaction occur faster (not necessarily more effectively, creating more product, but it decreases the amount of time it takes).
In chemistry, yes...yes it is.
If the totaling of bromine to cis-cinnamic acid uses the
same mechanism or device as the addition to trans-cinnamic acid, addition of
bromine only transpires on the top (syn) and not the bottommost face (anti). Therefore,
bromine added to cis-cinnamic only adds to the same face (syn addition) as a
result producing only threo dibromides.