Thank you for registering.

One of our academic counsellors will contact you within 1 working day.

Please check your email for login details.

Use Coupon: CART20 and get 20% off on all online Study Material

Total Price: Rs.

There are no items in this cart.
Continue Shopping

what are different types of reducing agents for reduction of aldehydes&ketones to alcohols

what are different types of reducing agents for reduction of aldehydes&ketones to alcohols


2 Answers

vineet chatterjee
42 Points
6 years ago
The reaction product of the reduction of an aldehyde is a primary alcohol and that of a ketone a secondary alcohol. Reagents are lithium aluminium hydride,diisobutylaluminium hydridesodium borohydride and aluminum hydride. Sodium borohydride tolerates more functional groups (nitro group,nitrileester) than LiAlH4 and can also be used with water or ethanol as a solvent (LiAlH4 reacts with protic solvents).Please approve the answer if you find it useful.
20 Points
6 years ago

The reduction of an aldehyde

You get exactly the same organic product whether you use lithium tetrahydridoaluminate or sodium tetrahydridoborate.

For example, with ethanal you get ethanol:

Notice that this is a simplified equation - perfectly acceptable to UK A level examiners. [H] means "hydrogen from a reducing agent".

In general terms, reduction of an aldehyde leads to a primary alcohol.


The reduction of a ketone

Again the product is the same whichever of the two reducing agents you use.

For example, with propanone you get propan-2-ol:

Reduction of a ketone leads to a secondary alcohol.


Using lithium tetrahydridoaluminate (lithium aluminium hydride)

Lithium tetrahydridoaluminate is much more reactive than sodium tetrahydridoborate. It reacts violently with water and alcohols, and so any reaction must exclude these common solvents.

The reactions are usually carried out in solution in a carefully dried ether such as ethoxyethane (diethyl ether). The reaction happens at room temperature, and takes place in two separate stages.

In the first stage, a salt is formed containing a complex aluminium ion. The following equations show what happens if you start with a general aldehyde or ketone. R and R' can be any combination of hydrogen or alkyl groups.

The product is then treated with a dilute acid (such as dilute sulphuric acid or dilute hydrochloric acid) to release the alcohol from the complex ion.

The alcohol formed can be recovered from the mixture by fractional distillation.

Using sodium tetrahydridoborate (sodium borohydride)

Sodium tetrahydridoborate is a more gentle (and therefore safer) reagent than lithium tetrahydridoaluminate. It can be used in solution in alcohols or even solution in water - provided the solution is alkaline.

I have a problem over describing the reaction conditions, because it seems to be used in so many different ways. Practical details found from various university sites vary widely, and don't necessarily agree with what theoretical sources say!

In what follows, I am choosing one out of many different methods. I have chosen this one largely because I think I understand what is going on!

Solid sodium tetrahydridoborate is added to a solution of the aldehyde or ketone in an alcohol such as methanol, ethanol or propan-2-ol. Depending on which recipe you read, it is either heated under reflux or left for some time around room temperature. This almost certainly varies depending on the nature of the aldehyde or ketone.

At the end of this time, a complex similar to the previous one is formed.

In the second stage of the reaction, water is added and the mixture is boiled to release the alcohol from the complex.

Again, the alcohol formed can be recovered from the mixture by fractional distillation.

Think You Can Provide A Better Answer ?

Provide a better Answer & Earn Cool Goodies See our forum point policy


Get your questions answered by the expert for free