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प्रश्न
Compounds A and C in the following reaction are:
\[\ce{CH3CHO ->[(i) CH3MgBr][(ii) H2O] (A) ->[H2SO4, Δ] (B) ->[Hydroboration oxidation] (C)}\]
पर्याय
identical
positional isomers
functional isomers
optical isomers
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उत्तर
positional isomers
Explanation:
Thus, \[\begin{array}{cc}
\ce{CH3CH - OH}\\
|\phantom{....}\\
\ce{CH3}\phantom{..}
\end{array}\] and \[\ce{CH3 - CH2 - CH2OH}\] are positional isomers.
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संबंधित प्रश्न
What is meant by the following term? Give an example of the reaction in the following case.
Aldol
How will you convert ethanal into the following compound?
Butane-1, 3-diol
How will you convert ethanal into the following compound?
But-2-enal
How will you bring about the following conversion in not more than two steps?
Benzaldehyde to 3-Phenylpropan-1-ol
Give reasons Acetylation of aniline reduces its activation effect.
Why is alpha (α) hydrogen of carbonyl compounds acidic in nature?
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) \[\begin{array}{cc}
\phantom{}\ce{CH3}\\
|\phantom{...}\\
\ce{CH3 - C - CHO}\phantom{..}\\
|\phantom{...}\\
\phantom{}\ce{CH3}\\
\end{array}\]
Which of the following conversions can be carried out by Clemmensen Reduction?
(i) Benzaldehyde into benzyl alcohol
(ii) Cyclohexanone into cyclohexane
(iii) Benzoyl chloride into benzaldehyde
(iv) Benzophenone into diphenyl methane
Compound ‘A’ was prepared by oxidation of compound ‘B’ with alkaline \[\ce{KMnO4}\]. Compound ‘A’ on reduction with lithium aluminium hydride gets converted back to compound ‘B’. When compound ‘A’ is heated with compound B in the presence of \[\ce{H2SO4}\] it produces fruity smell of compound C to which family the compounds ‘A’, ‘B’ and ‘C’ belong to?
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.
Cross aldol condensation occurs between
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:
What is aldol condensation? Explain it with suitable examples.
