Carboxylic Acid and Acid DerivativesHard
Question
The product obtained is /are
Options
A.o-product
B.m-product
C.o-and p-products
D.o-, m- and p-product
Solution
The phenol esters on treatment with AlCl3 (anhy.) undergoes rearrangement to give o- and p-hydroxyketones (Fries rearrangement)
Create a free account to view solution
View Solution FreeTopic: Carboxylic Acid and Acid Derivatives·Practice all Carboxylic Acid and Acid Derivatives questions
More Carboxylic Acid and Acid Derivatives Questions
The compound that does NOT liberate CO2, on treatment with aqueous sodium bicarbonate solution,is -...Among the given compounds, the most susceptible to nucleophilic attack at the carbonyl group is -...H2N − CH2 − CH2 − NH2 when reacts with diethyl oxalate gives...Rank the following compounds in order of increasing acidic strength :-(I) (II) (III)...What would happen when a solution of potassium chromate is treated with an excess of dilute nitric acid?...