मराठी
कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

CHX3CHX2OH can be converted into CHX3CHO by ______.

Advertisements
Advertisements

प्रश्न

\[\ce{CH3CH2OH}\] can be converted into \[\ce{CH3CHO}\] by ______.

पर्याय

  • catalytic hydrogenation

  • treatment with \[\ce{LiAlH4}\]

  • treatment with pyridinium chlorochromate

  • treatment with \[\ce{KMnO4}\]

MCQ
रिकाम्या जागा भरा
Advertisements

उत्तर

\[\ce{CH3CH2OH}\] can be converted into \[\ce{CH3CHO}\] by treatment with pyridinium chlorochromate.

Explanation:

Alcohols are oxidized to aldehydes and finally to acids.

\[\ce{CH3CH2OH ->[{[O]}] CH3CHO ->[{[O]}] CH3COOH}\]

Oxidations can be stooped at aldehyde stage by using pyridinium chlorochromate

\[\ce{(CrO3C5H5N.HCl)}\].

\[\ce{CH3CH2OH ->[PCC] CH3CHO}\]

shaalaa.com
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 11: Alcohols, Phenols and Ethers - Multiple Choice Questions (Type - I) [पृष्ठ १५४]

APPEARS IN

एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
पाठ 11 Alcohols, Phenols and Ethers
Multiple Choice Questions (Type - I) | Q 4 | पृष्ठ १५४

संबंधित प्रश्‍न

Give reasons for the following:

o-nitrophenol is more acidic than o-methoxyphenol.


Write the mechanism of the following reaction :


Write the mechanism of the following reaction :


Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of the corresponding phenoxide ions.


Give the equation of the following reaction:

Treating phenol with chloroform in the presence of aqueous NaOH.


Write the mechanism of acid-catalysed dehydration of ethanol to yield ethene.


Name the reagent used in the following reaction: 

Oxidation of a primary alcohol to carboxylic acid.


When 3-methylbutan-2-ol is treated with HBr, the following reaction takes place:

\[\begin{array}{cc}
\phantom{...................................}\ce{Br}\\
\phantom{..................................}|\\
\ce{CH3 - CH - CH - CH3 ->[HBr] CH3 - C - CH2 - CH3}\\
|\phantom{.........}|\phantom{...................................}|\phantom{...........}\\
\ce{CH3}\phantom{...}\ce{OH}\phantom{...............................}\ce{CH3}\phantom{.......}\\
\end{array}\]

Give a mechanism for this reaction.

(Hint: The secondary carbocation formed in step II rearranges to a more

stable tertiary carbocation by a hydride ion shift from 3rd carbon atom.)


Write the mechanism (using curved arrow notation) of the following reaction :


In the reduction \[\ce{R - CHO + H2 -> RCH2OH}\] the catalyst used is:


Dehydration of 2-butanol yields:


Which of the following is not true in case of reaction with heated copper at 300°C?


Identify the secondary alcohols from the following set:

  1. \[\ce{CH3CH2CH(OH)CH3}\]
  2. \[\ce{(C2H5)3COH}\]



The process of converting alkyl halides into alcohols involves ______.


Alcohols react with active metals e.g. Na, K etc. to give corresponding alkoxides. Write down the decreasing order of reactivity of sodium metal towards primary, secondary and tertiary alcohols.


Why is the C – O – H bond angle in alcohols slightly less than the tetrahedral angle whereas the C – O – C bond angle in ether is slightly greater?


Write the mechanism of acid dehydration of ethanol to yield ethene. 


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×