Reduction of benzophenone to diphenylethanol

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In summary, the reduction of benzophenone to diphenylmethanol involves the use of 4 moles of sodium borohydride, which donates a hydride to the carbonyl group and forms an intermediate with a negative charge on the oxygen atom. In the second stage of the reaction, water is added to release the alcohol from the complex. A balanced equation for this stage of the reaction can be written as NaBH4 + 4Benzophenone + H2O --> 4Diphenylmethanol + NaOH.
  • #1
Moogie
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Hi

When you are reducing benzophenone to diphenylethanol you use 4 moles of sodium borohydride. I don't know how you would write this as an equation because I don't know what the sodium borohydride becomes. It has lost 4 hydride ions and is just with a sodium and boron. Also, you haven't made the alcohol at this stage yet either - you have an intermediate with an O- species in it. YOu don't form the alchol until the acid work up step

How would i write a balanced equation for this stage of the reaction?

e.g. NaBH4 + 4Benzonphenone etc

thanks
 
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  • #2
Are you sure it is diphenyl'ethanol', not diphenyl'methanol' ?

NaBH4 is used to reduce carbonyl group to alcohol, or in other words, it donates a hydride. The hydride bonds with the carbon, and oxygen gets a negative charge. Now, a new complex is formed. You can see the reaction here: http://www.chemguide.co.uk/organicprops/carbonyls/nabh4eq1.gif

In the second stage of the reaction, water is added and the mixture is boiled to release the alcohol from the complex.
http://www.chemguide.co.uk/organicprops/carbonyls/nabh4eq2.gif


Source: http://www.chemguide.co.uk/organicprops/carbonyls/reduction.html

Hope this helps :)
 
  • #3
It was methanol - my mistake. Thanks for the link
 

Related to Reduction of benzophenone to diphenylethanol

1. What is the purpose of reducing benzophenone to diphenylethanol?

The reduction of benzophenone to diphenylethanol is a common reaction used in organic chemistry to synthesize alcohols. This reaction is often used to create a new carbon-carbon bond and can also be used to purify or isolate compounds.

2. What are the reagents and conditions required for this reduction?

The reduction of benzophenone to diphenylethanol typically requires a strong reducing agent such as sodium borohydride or lithium aluminum hydride. The reaction is usually carried out in a solvent such as ethanol or tetrahydrofuran at room temperature or under reflux conditions.

3. What are the potential side reactions during this reduction?

Some potential side reactions that may occur during the reduction of benzophenone to diphenylethanol include over-reduction, which can lead to the formation of byproducts such as diphenylmethanol, and competing reactions with other functional groups present in the molecule.

4. What are some applications of benzophenone to diphenylethanol reduction?

The reduction of benzophenone to diphenylethanol has many applications in organic synthesis, such as the preparation of pharmaceuticals, fragrances, and other industrial chemicals. It can also be used as a step in the synthesis of other compounds, such as diphenylmethanol and diphenylmethane derivatives.

5. Are there any safety precautions to consider when performing this reduction?

As with any chemical reaction, it is important to follow proper safety precautions when performing the reduction of benzophenone to diphenylethanol. This includes wearing appropriate personal protective equipment, working in a well-ventilated area, and properly disposing of any waste materials. It is also important to be familiar with the properties of the reagents and follow the recommended handling procedures.

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