Chemistry, asked by PragyaTbia, 1 year ago

How will you bring about the following conversions in not more than two steps? Benzaldehyde to 3-Phenylpropan-1-ol

Answers

Answered by tiwaavi
3

This Reaction can also be done in 2 steps.

Step 1 ⇒  When Benzaldehyde Reacts with the Aceytaldehyde, it will form CHCHCHOC₆H₅.

Reaction will be,

 C₆H₅CHO + CH₃CHO -----NaOH----- CHCHCHOC₆H₅.


Step 2 ⇒ When this formed compound reacts with the Hyudrogen in the Presence of the Renley Nickel or Ni at 200°C.

Reaction is,

CHCHCHOC₆H₅  +  H₂ ------------ C₆H₅CH₂CH₂CH₂OH


Refers to the attachment for the Diagrammatically Representation.


Hope it helps.

Attachments:
Answered by Arslankincsem
0

The Benzaldehyde which is a Benzene ring attached to the CHO compound will react in the presence of NaOH.


It will give out the Benzene ring with one carbon attached to CH=CHCHO.


This will further have catalytic hydrogenation or Ni/H2 which will give 3-phenylpropan-1-ol which will be the Benzene ring with CH2CH2CH2OH.

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