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प्रश्न
Maltose is a
(a) Polysaccharide
(b) Disaccharide
(c) Trisaccharide
(d) Monosaccharide
उत्तर
Disaccharide
APPEARS IN
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 is treated with bromine water?
Answer the following question.
What is the basic structural difference between glucose and fructose?
Write the reactions involved when D-glucose is treated with the following reagent:
(CH3CO)2O
The following compound can be called as:
Choose the appropriate answer(s) for the below representation from the options given
Acetylation of glucose yields ____________.
Which one of the following compounds is different from the rest?
When glucose reacts with bromine water, the main product is ____________.
Glucose reacts with acetic anhydride to form ______.
Glucose is found to exist in two different α and β crystalline forms. These forms can be obtained by:
(i) The α form of glucose is obtained by crystallisation from a concentrated solution of glucose at 303 K.
(ii) The β form of glucose is obtained by crystallisation from a concentrated solution of glucose at 303 K.
(iii) The β form is obtained by crystallisation from hot and saturated aqueous solution at 371 K.
(iv) The α form is obtained by crystallisation from hot and saturated aqueous solution at 371 K.
The reaction of glucose with red P + HI is called ____________.
Which of the following reactions of glucose can be explained only by its cyclic structure?
Which is the least stable form of glucose?
The letter D and L in carbohydrates represent ____________.
Which one of the following reactions is not explained by the open chain Structure of glucose?
In the following reaction, identify A and B:
\[\begin{array}{cc}
\ce{C6H12O6 ->[Acetic anhydride] A}\\
\downarrow \text{Conc. nitric acid}\phantom{...}\\
\ce{B}\phantom{.................}\end{array}\]
Why does compound (A) given below not form an oxime?
(A)
Write the reactions of D-glucose which can’t be explained by its open-chain structure. How can cyclic structure of glucose explain these reactions?
What happens when D-glucose is treated with the following reagent?
HI
Account for the following:
What happens when D – glucose is treated with the following reagents
Bromine water
Account for the following:
What happens when D – glucose is treated with the following reagents
HNO3
Consider the following reactions:
(i) \[\ce{Glucose + R-OH ->[Conc. HNO3] [A] ->[X eq of][(CH3CO)2O] Acetyl derivative}\]
(ii) \[\ce{Glucose ->[Ni/H2] [A] ->[Y eq of][(CH3CO)2O] Acetyl derivative}\]
(iii) \[\ce{Glucose ->[Z eq of][(CH3CO)2O] Acetyl derivative}\]
'X, 'Y' and 'Z' in these reactions are respectively:
Glucose with excess of phenyl hydrazine forms ______.
Match List - I with List - II.
| List I | List II | ||
| (A) | Glucose + HI | (I) | Gluconic acid |
| (B) | Glucose + Br2 water | (II) | Glucose pentacetate |
| (C) | Glucose + acetic anhydride | (III) | Saccharic acid |
| (D) | Glucose + HNO3 | (IV) | Hexane |
Choose the correct answer from the options given below:
When D-glucose reacts with HI, it forms ______.
