Fructose reduces Tollen's reagent due to:
| 1. | Primary alcoholic group |
| 2. | Secondary alcoholic group |
| 3. | Enolisation of fructose followed by conversion to aldehyde by base |
| 4. | Asymmetric carbon |
Monosaccharides are:
| 1. | Carbohydrates that can't be hydrolysed further to give simpler units of polyhydroxy aldehyde or ketone. |
| 2. | Classified on the basis of the number of carbon atoms and the functional group present in them. |
| 3. | The monomers of carbohydrates. |
| 4. | All of the above. |
Glucose and Fructose can be distinguished by the use of :
1. Fehling solution
2. Tollen's reagent
3. Bromine water
4. All of the above
| a. | Glucose is also known as dextrose. |
| b. | Glucose is oxidized to saccharic acid using bromine water. |
| c. | \(\alpha - \text D (+) -\) Glucose contains five chiral centers. |
The major product obtained when glucose reacts with bromine water among the following is:
1. Gluconic acid
2. Glyceraldehyde
3. Sorbitol
4. Saccharic acid
D-glucose upon treatment with nitric acid gives:
| 1. | |
2. | ![]() |
| 3. | ![]() |
4. | ![]() |
Which one is not a D-sugar:
| 1. | 2. | ||
| 3. | 4. |
D configuration is shown by:
| (i) | (ii) | (iii) |
1. i, ii and iii
2. ii and iii
3. i and ii
4. Only iii
| 1. | C1 | 2. | C2 and C3 |
| 3. | C4 and C5 | 4. | C6 |
The incorrect statement among the following regarding glucose is:
| 1. | It is an aldohexose. |
| 2. | n-Hexane is formed when glucose is heating with HI. |
| 3. | It is present in furanose form. |
| 4. | It does not give 2, 4- DNP test. |