Final answer:
The product of CH3CH2CH2CH2Li with various compounds depends on the compounds it reacts with, but typical reactions include deprotonation of acidic compounds and nucleophilic addition to electrophilic centers, resulting in alcohols after protonation.
Step-by-step explanation:
The product formed when CH3CH2CH2CH2Li is treated with each compound would vary depending on the compound it is reacting with. Since the specific compounds are not provided in the question, I cannot draw the specific products. However, CH3CH2CH2CH2Li is an organolithium reagent, which is typically used as a strong base and nucleophile in organic synthesis. It can be used to deprotonate acidic compounds and to perform nucleophilic addition reactions with electrophilic carbon centers.
For example, in reaction with a simple carbonyl compound like an aldehyde or ketone, CH3CH2CH2CH2Li would perform a nucleophilic addition to the electrophilic carbon of the carbonyl group. The result would be the formation of an alcohol after subsequent protonation.
The SEO keywords chosen for this response are nucleophilic addition, organolithium reagent, and alcohol.