Answer :
Final answer:
The Burgess reagent reaction with alcohol typically involves the dehydration of alcohols to alkenes, though this is not explicitly described in the information provided. Instead, we have details on the reactions of Grignard reagents with various compounds to produce alcohols.
Explanation:
The reaction of Burgess reagent on alcohol is not directly described in the information provided. However, the Burgess reagent is typically used for the dehydration of alcohols to give alkenes. In these reactions, the alcohol reacts with the Burgess reagent to form a sulfonamide intermediate, which undergoes an E2 elimination to yield the alkene product.
To discuss the reaction of alcohols with other reagents as mentioned in the supplied information, we observe different outcomes. For instance, reacting a Grignard reagent with ethylene oxide produces a primary alcohol with a two-carbon increase in the chain. Likewise, the reaction of a Grignard reagent with a ketone results in the formation of an alcohol, where aldehydes and ketones offer a nucleophilic addition site for the Grignard reagent, leading to the formation of secondary or tertiary alcohols, respectively.
