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Question
Write the structures of A and B in the following reactions
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Solution
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RELATED QUESTIONS
Predict the products of the following reactions:
Show how the following compound can be converted to benzoic acid.
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Show how the following compound can be converted to benzoic acid.
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How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.
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How will you bring about the following conversion in not more than two steps?
Benazaldehyde to α-Hydroxyphenylacetic acid
Match the reactions given in Column I with the suitable reagents given in Column II.
| Column I (Reactions) |
Column II (Reagents) |
| (i) Benzophenone Diphenylmethane | (a) \[\ce{LiAlH4}\] |
| (ii) Benzaldehyde 1-Phenylethanol | (b) \[\ce{DIBAL-H}\] |
| (iii) Cyclohexanone Cyclohexanol | (c) \[\ce{Zn(Hg)/Conc. HCl}\] |
| (iv) Phenyl benzoate Benzaldehyde | (d) \[\ce{CH3MgBr}\] |
The end product Y in the sequence of reaction:
\[\ce{RX ->[CN^-] X ->[NaOH] Y}\] is:
Alkaline hydrolysis of C4H8Cl2 gives a compound (A) which on heating with NaOH and I2 produces a yellow precipitate of CHI3. The compound (A) should be ______.
A compound 'X' with molecular formula C3H8O can be oxidised to a compound 'Y' with the molecular formula C3H6O2 'X' is most likely to be ______.
Fill in the blanks by choosing the appropriate words from those given in the brackets:
[stable, low, aldehyde, unstable, 6, 4, ethane, Clemmensen’s, 2, 3, carboxylic acid, high, propane, Rosenmund's]
The primary alcohols are easily oxidised first into ______ and then into ______.
