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प्रश्न
When D-glucose reacts with HI, it forms ______.
पर्याय
Gluconic acid
n-hexane
Saccharic acid
Iodohexane
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उत्तर
When D-glucose reacts with HI, it forms n-hexane.
Explanation:
On prolonged heating with HI, it forms n-hexane, suggesting that all the six carbon atoms are linked in a straight chain.
\[\begin{array}{cc}
\ce{CHO}\phantom{.................................................}\\
|\phantom{.....................................................}\\
\ce{(CHOH)4 ->[HI,\Delta] \underset{{(n-Hexane)}}{CH3 - CH2 - CH2 - CH2 - CH2 - CH3}}\\
|\phantom{.....................................................}\\
\ce{CH2OH}\phantom{...............................................}
\end{array}\]
APPEARS IN
संबंधित प्रश्न
Draw the simple Fisher projection formulae of D - (+) - glucose and D - (-) - fructose
Enlist the properties of glucose that can not be explained on the basis of open chain structure of it
Answer the following question.
What is the basic structural difference between glucose and fructose?
The number of asymmetric carbon atom(s) below the figure is/are


Oxime is formed by treating glucose with ____________.
Which of the following statements is incorrect regarding glucose?
Which one of the following compounds is different from the rest?
The number of chiral carbon atoms present in cyclic structure α-D(+) glucose:
The two forms of D-glucopyranose obtained from the solution of D-glucose are called ____________.
In the following reaction, identify A and B:
\[\begin{array}{cc}
\ce{C6H12O6 ->[Acetic anhydride] A}\\
\downarrow \text{Conc. nitric acid}\phantom{...}\\
\ce{B}\phantom{.................}\end{array}\]
