Alcohol Reactions - HBr, PBr3, SOCl2 | Summary and Q&A

TL;DR

The video discusses the reactions and mechanisms involved in converting alcohols into alkyl halides using different reagents.

Key Insights

• 🫀 Alcohol reactions with hydrobromic acid result in the conversion of the OH group to a bromine atom in alkyl halides.
• 💁 Primary alcohols undergo SN2 reactions, while secondary and tertiary alcohols undergo SM1 reactions to form alkyl halides.
• ❓ Zinc chloride can enhance the reaction of primary alcohols with hydrochloric acid.
• ❓ PBr3 and SOCl2 are reagents that can convert alcohols into alkyl halides through SN2 mechanisms.
• 🥺 Different reaction mechanisms lead to different stereochemistry outcomes.
• ❓ The Lucas reagent, zinc chloride, and pyridine are commonly used in alcohol conversion reactions.

Transcript

in this video we're going to go over reactions associated with alcohols so what's going to happen if we react in alcohol with hydrobromic acid the oh group will be replaced with a bromine atom so that's going to be the end result and so basically the alcohol is converted into an alkyl halide but now let's go over the mechanism for this reaction now... Read More

Questions & Answers

Q: What happens when an alcohol reacts with hydrobromic acid?

The OH group is replaced with a bromine atom, resulting in the conversion of the alcohol into an alkyl halide through an SN2 reaction mechanism.

Q: Why do primary alcohols react slowly with hydrochloric acid?

Primary alcohols react slowly with hydrochloric acid because chloride is a weaker nucleophile than bromide. However, the reaction can be enhanced by using zinc chloride, known as the Lucas reagent.

Q: How does the mechanism differ for converting a tertiary alcohol into an alkyl halide?

The mechanism for converting a tertiary alcohol into an alkyl halide involves an SM1 reaction. The hydroxyl group is first protonated to form a good leaving group, followed by the attack of the halide ion on the resulting carbocation.

Q: What reagents can be used to convert alcohols into alkyl halides through SN2 mechanisms?

Reagents like PBr3 and SOCl2 can be used to convert alcohols into alkyl halides through SN2 mechanisms, where the OH group is replaced by a bromine atom or a chlorine atom, respectively.

Summary & Key Takeaways

• Alcohols can be converted into alkyl halides by replacing the OH group with a halogen atom.

• Primary alcohols undergo an SN2 reaction with hydrobromic acid, while secondary and tertiary alcohols undergo SM1 reactions with different reagents.

• Other reagents like PBr3 and SOCl2 can also be used to convert alcohols into alkyl halides through SN2 mechanisms.