English

The product of following reaction is CHA3−CH=CH−CHA2−CHO→ii) HA3OA+i) LiAlHA4 ______? - Chemistry

Advertisements
Advertisements

Question

The product of following reaction is

\[\ce{CH3 - CH = CH - CH2 - CHO ->[i) LiAlH4][ii) H3O+]}\] ______?

Options

  • CH3 – CH2 – CH2 – CH2 – CH2 – OH

  • CH3 – CH = CH – CH2 – CH2 – OH

  • CH3 – CH2 – CH2 – CH2 – COOH

  • CH3 – CH = CH – CH2 – COOH

MCQ
Fill in the Blanks

Solution

The product of following reaction is

\[\ce{CH3 - CH = CH - CH2 - CHO ->[i) LiAlH4][ii) H3O+]}\] CH3 – CH = CH – CH2 – CH2 – OH.

shaalaa.com
  Is there an error in this question or solution?
2022-2023 (March) Official

RELATED QUESTIONS

Arrange the following compounds in increasing order of their property as indicated:

Acetaldehyde, Acetone, Di-tert-butyl ketone, Methyl tert-butyl ketone (reactivity towards HCN)


How are the following compounds prepared?

benzaldehyde from benzoyl chloride


Write balanced chemical equations for action of ammonia on - acetaldehyde


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"`


What are amines?


How will you convert benzoic acid to m-bromobenzoic acid?


Benzaldehyde can be obtained from benzal chloride. Write reactions for obtaining benzalchloride and then benzaldehyde from it.


Alkenes   and carbonyl compounds , both contain a π bond but alkenes show electrophilic addition reactions whereas carbonyl compounds show nucleophilic addition reactions. Explain.


Carboxylic acids contain carbonyl group but do not show the nucleophilic addition reaction like aldehydes or ketones. Why?


Acetaldehyde and acetone differ in their reaction with


The most stable reagent for the conversion of R – CH2OH → RCHO is


What happens when propanone is treated with CH3MgBr and then hydrolysed?


Which will undergo faster nucleophilic addition reaction?

Acetaldehyde or Propanone


In the following reaction

\[\ce{Carbonyl compound + MeOH <=>[HCl] acetal}\]

Rate of the reaction is the highest for ______.


Which of the following is most reactive in nucleophilic addition reactions?


Write the structure of the product formed when acetone reacts with 2, 4 DNP reagent.


Draw structures of the given derivatives.

The ethylene ketal of hexan-3-one


Draw structures of the given derivatives.

The ethylene ketal of hexan-3-one


Why dissociation of HCN is suppressed by the addition of HCL?


Draw structures of the following derivative.

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 structure of the following derivative:

Acetaldehydedimethylacetal


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one 


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×