SOLVED: In the synthesis of t-butyl chloride, explain why HCl is addedto form an acidic environment.If t-butanol was a chiral molecule, what would you expect toobtain as a product?Do you expect the nucleophile to affect the rate of anSN1 reaction? SN2? Why?Use an online resource like the NIST chemistry web book andfind IR spectra for both t-butanol and 1-butanol? If the reactionswere successful what do you expect to see in the IR of the productcompared to the starting material?Use an online reso

Williamson Ether Synthesis - Mechanism, Uses, Limitations & Reaction Conditions

Tertiary butyl alcohol gives tertiary butyl chloride on treatment with:

Acyl Chloride Uses, Reactions & Synthesis

▷ Claisen-Schmidt condensation | Chemistry Online

SOLVED: When the reaction of tosyl chloride and an alcohol is performed with triethyl amine instead of pyridine, an unwanted byproduct is often formed in small quantities. Propose a mechanism (show arrow-pushing) that can account for the byproduct formation. Include a BRIEF rationale/explanation for your mechanism (explain the key points and why it makes sense to you). (15 pts)(Tosyl chloride)(Desired product)(Undesired byproduct)(Triethyl amine)