key term - Sodium Borohydride

Definition

Sodium borohydride is a powerful reducing agent commonly used in organic chemistry reactions to reduce carbonyl compounds to alcohols. It is a versatile reagent that finds applications in various topics, including the reduction of aromatic compounds, the preparation of alcohols, the synthesis of ethers, and the nucleophilic addition of hydride to carbonyl groups.

5 Must Know Facts For Your Next Test

1. Sodium borohydride is a mild and selective reducing agent, making it useful for the reduction of aromatic compounds without affecting the aromatic ring.
2. In the preparation of alcohols, sodium borohydride can be used to reduce carbonyl compounds, such as aldehydes and ketones, to the corresponding alcohols.
3. Sodium borohydride is a key reagent in the synthesis of ethers, where it is used to reduce alkyl halides to the corresponding alcohols, which can then be converted to ethers.
4. The nucleophilic addition of hydride from sodium borohydride to carbonyl groups is a common method for the formation of alcohols.
5. Sodium borohydride is a relatively mild reducing agent compared to other hydride sources, such as lithium aluminum hydride, making it a safer and more selective choice for many organic transformations.

Review Questions

• Explain how sodium borohydride can be used in the reduction of aromatic compounds.
  • Sodium borohydride is a selective reducing agent that can be used to reduce aromatic compounds without affecting the aromatic ring structure. This is particularly useful in organic synthesis, where the preservation of the aromatic system is often desired. The mild and chemoselective nature of sodium borohydride allows for the reduction of functional groups, such as nitro or carbonyl groups, on aromatic compounds while leaving the aromatic core intact.
• Describe the role of sodium borohydride in the preparation of alcohols from carbonyl compounds.
  • Sodium borohydride is a commonly used reagent for the reduction of carbonyl compounds, such as aldehydes and ketones, to the corresponding alcohols. This transformation is a key step in the preparation of alcohols, as it allows for the conversion of readily available carbonyl precursors into valuable alcohol products. The nucleophilic addition of the hydride from sodium borohydride to the electrophilic carbonyl carbon results in the formation of a tetrahedral intermediate, which then collapses to yield the desired alcohol.
• Analyze the role of sodium borohydride in the synthesis of ethers, considering its use in the preparation of alcohols and their subsequent conversion to ethers.
  • Sodium borohydride plays a crucial role in the synthesis of ethers by first reducing alkyl halides to the corresponding alcohols. This is achieved through the nucleophilic addition of the hydride from sodium borohydride to the electrophilic carbon of the alkyl halide, resulting in the formation of an alcohol. These alcohols can then be further transformed into ethers through various methods, such as the Williamson ether synthesis. The ability of sodium borohydride to selectively reduce alkyl halides to alcohols, without affecting other functional groups, makes it a valuable tool in the preparation of ethers.

Related terms

Reducing Agent:

A reducing agent is a substance that has the ability to donate electrons, thereby reducing other substances and getting oxidized itself.

Carbonyl Compound:

Carbonyl compounds are organic compounds containing a carbon-oxygen double bond, such as aldehydes, ketones, carboxylic acids, and esters.

Nucleophilic Addition:

Nucleophilic addition is a type of organic reaction where a nucleophile adds to the electrophilic carbon of a carbonyl group, forming a tetrahedral intermediate.