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प्रश्न
Write the product formed on reaction of D-glucose with Br2 water.
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उत्तर
Br2 water oxidises D- glucose into D- gluconic acid.

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संबंधित प्रश्न
What happens when \[\ce{CH3 - Br}\] is treated with KCN?
Chlorobenzene is extremely less reactive towards a nucleophilic substitution reaction. Give two reasons for the same.
How the following conversion can be carried out?
Chlorobenzene to p-nitrophenol
Give reasons:
The dipole moment of chlorobenzene is lower than that of cyclohexyl chloride.
What is Grignard reagent?
Which of the following compounds will give racemic mixture on nucleophilic substitution by \[\ce{OH-}\] ion?
(a) \[\begin{array}{cc}
\phantom{}\ce{CH3 - CH - Br}\\
\phantom{}|\\
\phantom{....}\ce{C2H5}\phantom{}
\end{array}\]
(b) \[\begin{array}{cc}
\phantom{..}\ce{Br}\\
\phantom{}|\\
\phantom{}\ce{CH3 - C - CH3}\\
\phantom{}|\\
\phantom{....}\ce{C2H5}\phantom{}
\end{array}\]
(c) \[\begin{array}{cc}
\phantom{....}\ce{CH3 - CH - CH2Br}\\
\phantom{}|\\
\phantom{....}\ce{C2H5}\phantom{}
\end{array}\]
Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
| (a) | ![]() |
| (b) | ![]() |
| (c) | ![]() |
Haloarenes are less reactive than haloalkanes and haloalkenes. Explain.
Assertion: Chlorobenzene is resistant to nucleophilic substitution reaction at room temperature.
Reason (R): C–Cl bond gets weaker due, to resonance.
In the reaction, \[\mathrm{CH}_3\mathrm{C}\equiv\mathrm{\overline{C}Na}^++(\mathrm{CH}_3)_2\mathrm{CHCl}\to\] the product formed is ______.



