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प्रश्न
Write the reactions involved when D-glucose is treated with the following reagent:
H2N-OH
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उत्तर
\[\begin{array}{cc}
\phantom{............}\ce{CHO}\phantom{.............}\ce{CO=N-OH}\\
\phantom{..}|\phantom{..................}|\\
\phantom{........}\ce{(CHOH)4->[NH2OH](CHOH)4}\\
\phantom{..}|\phantom{..................}|\\
\phantom{.........}\ce{\underset{\text{D-glucose}}{CH2OH}}\phantom{..........}\ce{\underset{\text{Oxime}}{CH2OH}}
\end{array}\]
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संबंधित प्रश्न
Draw the simple Fisher projection formulae of D - (+) - glucose and D - (-) - fructose
Enumerate the reactions of D-glucose which cannot be explained by its open chain structure.
What do you observe when glucose solution is heated with Tollen’s reagent?
Choose the appropriate answer(s) for the below representation from the options given
Which one of the following compounds is different from the rest?
Which of the following reactions of glucose can be explained only by its cyclic structure?
Which of the following pairs represents anomers?
Why does compound (A) given below not form an oxime?
(A)
How will you distinguish 1° and 2° hydroxyl groups present in glucose? Explain with reactions.
Give a reason for the following observations:
Penta-acetate of glucose does not react with hydroxylamine.
