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प्रश्न
Draw the simple Fisher projection formulae of D - (+) - glucose and D - (-) - fructose
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उत्तर


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संबंधित प्रश्न
Write the reaction that indicates the presence of -CHO group in glucose
How many moles of acetic anhydride will be required to form glucose pentaacetate from 2M of glucose?
(a) 2
(b) 5
(c) 10
(d) 2.5
What happens when glucose is treated with hydroxylamine?
Glucose on reaction with HI gives n-hexane. What does it suggest about the structure of glucose?
The following compound can be called as:

Choose the appropriate answer(s) for the below representation from the options given


Which of the following statements is incorrect regarding glucose?
The symbols D and L represents ____________.
Which one of the following compounds is different from the rest?
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 is the least stable form of glucose?
A solution of D-glucose in water rotates the plane polarised light ____________.
The number of chiral carbon atoms present in cyclic structure α-D(+) glucose:
The number of chiral carbons in ß-D(+) glucose is ____________.
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.
Assertion: D (+) – Glucose is dextrorotatory in nature.
Reason: ‘D’ represents its dextrorotatory nature.
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:
There are 5 OH groups in glucose
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:
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 ______.
Give the reaction of glucose with hydrogen cyanide. Presence of which group is confirmed by this reaction?
The reagents with which glucose does not react to give the corresponding tests/products are:
- Tollen’s reagent
- Schiff’s reagent
- HCN
- NH2OH
- NaHSO3
Choose the correct options from the given below:
