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

Write structural formulas and names of four possible aldol condensation products from propanal and butanal. In each case, indicate which aldehyde acts as nucleophile and which as electrophile. - Chemistry

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प्रश्न

Write structural formulas and names of four possible aldol condensation products from propanal and butanal. In each case, indicate which aldehyde acts as nucleophile and which as electrophile.

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अति संक्षिप्त उत्तर
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उत्तर

The possible products of aldol condensation from propanal and butanal are:

(i) \[\begin{array}{cc}
\phantom{..............................}\ce{OH}\phantom{...}\ce{CH3}\\
\phantom{...........................}|\phantom{.....}|\\
\ce{\underset{Propanal}{2CH3CH2CHO}->[dil.\overset{-}{O}H]\underset{3-Hydroxy-2-methylpentanal}{H3C - CH2 - CH - CH - CHO}}\\
\end{array}\]

(ii) \[\begin{array}{cc}
\phantom{.......................................}\ce{OH}\phantom{..}\ce{CH2CH3}\\
\phantom{................................}|\phantom{.....}|\\
\ce{\underset{Butanal}{2CH3(CH2)2CHO}->[dil.\overset{-}{O}H]\underset{2-Ethyl-3-hydroxyhexanal}{H3C - (CH2)2 - CH - CH - CHO}}\
\end{array}\]

(iii) When butanal acts as an electrophile and propanal as a nucleophile:

\[\begin{array}{cc}
\phantom{...........................................}\ce{OH}\\
\phantom{.........................................}|\\
\ce{\underset{Butanal}{H3C - (CH2)2CHO} + \underset{Propanal}{CH3CH2CHO}->[\overset{-}{O}H]H3C - (CH2)2 - CH - CH - CHO}\\
\phantom{.....................................................}|\\
\phantom{.........................................................}\ce{\underset{3-Hydroxy-2-methylhexanal}{CH3}}\
\end{array}\]

(iv) When propanal serves as an electrophile and butanal as a nucleophile:

\[\begin{array}{cc}
\phantom{............................................}\ce{OH}\phantom{...}\ce{C2H5}\\
\phantom{.........................................}|\phantom{......}|\\
\ce{CH3CH2CHO + CH3(CH2)2CHO -> \underset{2-Ethyl-3-hydroxypentanal}{H3C - CH2 - CH - CH - CHO}}\
\end{array}\]

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पाठ 8: Aldehydes, Ketones and Carboxylic Acids - Exercises [पृष्ठ २५६]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
पाठ 8 Aldehydes, Ketones and Carboxylic Acids
Exercises | Q 8.9 | पृष्ठ २५६

संबंधित प्रश्‍न

Write the products formed when CH3CHO reacts with the following reagents: CH3CHO in the presence of dilute NaOH


Describe the following:

Cross aldol condensation


Complete the synthesis by giving missing starting material, reagent or product.

\[\begin{array}{cc}
\ce{C6H5CHO}\phantom{............}\\
\phantom{........}\ce{+\phantom{......}\ce{->[dil.NaOH][\Delta]}}\phantom{...}\\
\ce{CH3CH2CHO}\phantom{............}
\end{array}\]


 Why is alpha (α) hydrogen of carbonyl compounds acidic in nature?


Write chemical equations of the following reaction : 

Propanone is treated with dilute Ba (OH)2-.


Write chemical equations of the following reaction :
Benzoyl chloride is hydrogenated in the presence of `"Pd"/(BaSO_4)`


Write a chemical equation for the following reaction: 
Propanone is treated with dilute Ba( OH)2.


Which product is formed when the compound  is treated with concentrated aqueous \[\ce{KOH}\] solution?


Which of the following compounds do not undergo aldol condensation?

(i) \[\ce{CH3 - CHO}\]

(ii)  

(iii)  \[\begin{array}{cc}
\phantom{}\ce{O}\\
\phantom{}||\\
\ce{CH3 - C - CH3}
\end{array}\]

(iv) \[\begin{array}{cc}
\phantom{}\ce{CH3}\\
|\phantom{...}\\
\ce{CH3 - C - CHO}\phantom{..}\\
|\phantom{...}\\
\phantom{}\ce{CH3}\\
\end{array}\]


Assertion: The α-hydrogen atom in carbonyl compounds is less acidic.

Reason: The anion formed after the loss of α-hydrogen atom is resonance stabilised.


Give reasons to support the answer:

Presence of Alpha hydrogen in aldehydes and ketones is essential for aldol condensation.


Convert the following:

Acetaldehyde to But-2-enal


\[\ce{CH3-CH2-CHO ->[dil][alkali] Product}\]

The product in the above reaction is:


Explain Aldol condensation of ethanal.


Which of the following compounds will undergo self-condensation in the presence of dilute NaOH solution?


Why is the α-hydrogens of aldehydes and ketones are acidic in nature?


Identify A and B:


Write a note on the aldol condensation reaction of acetaldehyde.


What is aldol condensation? Explain it with suitable examples.


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