What is the Difference Between NaBH4 and LiAlH4 Reaction?
🆚 Go to Comparative Table 🆚The main difference between NaBH4 and LiAlH4 lies in their reactivity and the types of compounds they can reduce. Both NaBH4 and LiAlH4 are reducing agents, but LiAlH4 is a stronger reducing agent than NaBH4 due to the weaker Al-H bond in LiAlH4, which makes it more reactive. Here are some key differences between the two:
- Types of compounds they can reduce: NaBH4 can reduce aldehydes, ketones, and acid halides to the corresponding alcohols, but it generally cannot reduce esters. On the other hand, LiAlH4 can reduce esters, amides, and carboxylic acids, in addition to aldehydes and ketones.
- Reactivity: LiAlH4 is a more reactive reducing agent than NaBH4. This high reactivity of LiAlH4 makes it incompatible with protic solvents, and it reacts violently with water. NaBH4, being less reactive, can be used in the selective reduction of aldehydes and ketones in the presence of an ester.
- Mechanism: Both NaBH4 and LiAlH4 function as a source of hydride (H−), which acts as a nucleophile attacking the carbonyl group. However, the mechanisms for NaBH4 and LiAlH4 reductions are slightly different, particularly for ester reductions.
In summary, both NaBH4 and LiAlH4 are reducing agents used in organic synthesis, but they differ in their reactivity and the types of compounds they can reduce. LiAlH4 is generally more reactive and can reduce a wider range of compounds, including esters, amides, and carboxylic acids, while NaBH4 is less reactive and mainly reduces aldehydes, ketones, and acid halides.
Comparative Table: NaBH4 vs LiAlH4 Reaction
The main differences between the reactions of NaBH4 and LiAlH4 arise from their reactivity and the types of carbonyl compounds they can reduce. Here is a table summarizing the differences:
Reducing Agent | Reactivity | Reduction of Aldehydes and Ketones | Reduction of Esters | Reduction of Carboxylic Acids |
---|---|---|---|---|
NaBH4 (Sodium Borohydride) | Moderate | Reduces aldehydes and ketones to primary and secondary alcohols | Does not reduce esters | Not strong enough to reduce carboxylic acids or esters to alcohols |
LiAlH4 (Lithium Aluminum Hydride) | Stronger | Reduces aldehydes and ketones to primary and secondary alcohols | Reduces esters to primary alcohols | Reduces carboxylic acids to 1o alcohols |
NaBH4 is a moderate reducing agent and can be used for the selective reduction of aldehydes and ketones in the presence of esters. In contrast, LiAlH4 is a stronger reducing agent and can reduce a wider range of carbonyl compounds, including esters and carboxylic acids.
- LiAlH4 vs NaBH4
- Ammonium Hydroxide vs Sodium Hydroxide
- Sodium Hydroxide vs Potassium Hydroxide
- Alkali vs Alkaline
- Lithium Carbonate vs Lithium Hydroxide
- Ammonia vs Ammonium Hydroxide
- NH3N vs NH4N
- Alkali vs Acid
- Alkaline vs Lithium Batteries
- Lithium vs Other Alkali Metals
- Acid Anhydride vs Basic Anhydride
- Beryllium vs Lithium
- Alkali vs Base
- Hydrogen Bromide vs Hydrobromic Acid
- Alkylation vs Acylation
- Alpha vs Beta Elimination Reaction
- Balanced Equation vs Net Ionic Equation
- Reactant vs Reagent
- Lye vs Caustic Soda