Advertisements
Advertisements
Question
What is the action of the following reagents on ethanoic acid?
1) `LiAlH_4"/"H_3O^+`
2) `PCl_3 , "heat"`
3) `P_2O_5, "heat"`
Advertisements
Solution
1) \[\ce{\underset{\text{ethanoic acid}}{CH3} - COOH ->[LiAIH4IH3O+] \underset{\text{ethanol}}{CH3} -CH2-OH}\]
Ethanoic acid when treated with reducing agent like LiAlH4 , it gives ethanol
2) \[\ce{\underset{\text{ethanoic acid}}{3CH3 - COOH} - PCI3 ->[\Delta] \underset{\text{acetylcholoride}}{3CH3COCI + H3PO3}}\]
Ethanoic acid, when treated with PCl3, gives acetyl chloride
3) \[\ce{\underset{\text{two molecules of ethanoic acid}}{CH3COOH + CH3COOH} ⇌[P2O5][A] \underset{\text{acetic anhydride}}{(CH3 - CO)2O} + OH}\]
When two molecules of ethanoic acid heated with strong dehydrating agent P2O5, it removes water molecules to for acetic anhydride.
APPEARS IN
RELATED QUESTIONS
Write balanced chemical equations for action of ammonia on - formaldehyde
Predict the product of the following reaction:

Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents.
Semicarbazide and weak acid
Acetaldehyde, Acetone, Di-tert-butyl ketone, Methyl tert-butyl ketone (reactivity towards HCN)
How will you bring about the following conversion in not more than two steps?
Bromobenzene to 1-Phenylethanol
Complete the synthesis by giving missing starting material, reagent or product.
\[\ce{C6H5CHO ->[H2NCONHNH2]}\]
Explain the mechanism of alkaline hydrolysis of tert-butyl bromide with energy profile diagram.
Write balanced chemical equations for action of ammonia on - acetaldehyde
Write balanced chemical equations for action of ammonia on - acetone
Write balanced chemical equations for action of ammonia on - acetone
Acetone, Acetaldehyde, Benzaldehyde, Acetophenone – reactivity towards addition of HCN.
Which of the following compounds is most reactive towards nucleophilic addition reactions?
Carboxylic acids contain carbonyl group but do not show the nucleophilic addition reaction like aldehydes or ketones. Why?
Paraldehyde is formed as a result of polymerisation:-
Which among the following is most reactive to give nucleophilic addition?
Arrange the following in the increasing order of their property indicated:
Ethanal, Propanone, Propanal, Butanone (reactivity towards nucleophilic addition)
The product of following reaction is
\[\ce{CH3 - CH = CH - CH2 - CHO ->[i) LiAlH4][ii) H3O+]}\] ______?
Draw structures of the given derivatives.
The ethylene ketal of hexan-3-one
The product of the following reaction is
\[\begin{array}{cc}
\ce{O}\phantom{.........}\\
||\phantom{.........}\\
\ce{C2H5 - C - CH3 ->[H2/Ni][\Delta] \phantom{..}?}\end{array}\]
Draw the structure of the following derivative.
The ethylene ketal of hexan-3-one
Draw structures of the following derivatives.
Acetaldehydedimethylacetal
Draw structure of the following derivative.
The ethylene ketal of hexan-3-one
Draw structures of the given derivatives.
The ethylene ketal of hexan-3-one
Draw structure of the following derivative.
The ethylene ketal of hexan-3-one
Draw the structure of the given derivative.
The ethylene ketal of hexan-3-one
