The correct match between item I and item II is
| Item I (Compound) | Item II (Reagent) | ||
| a. | Lysine | p. | 1−naphthol |
| b. | Furfural | q. | Ninhydrin |
| c. | Benzyl alcohol | r. | KMnO4 |
| d. | Styrene | s. | Ceric ammonium nitrate |
Held on 10 Jan 2019 · Verified 6 Jul 2026.
a→q,b→r,c→s,d→p
a→q,b→p,c→s,d→r
a→r,b→p,c→q,d→s
a→q,b→p,c→r,d→s
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Identify the correct statements. A. Arginine and Tryptophan are essential amino acids. B. Histidine does not contain heterocyclic ring in its structure. C. Proline is a six membered cyclic ring amino acid. D. Glycine does not have chiral centre. E. Cysteine has characteristic feature of side chain as $\mathrm{MeS}-\mathrm{CH}_{2}-\mathrm{CH}_{2}-$. Choose the correct answer from the options given below :
The correct statements are : A. Activation energy for enzyme catalysed hydrolysis of sucrose is lower than that of acid catalysed hydrolysis. B. During denaturation, secondary and tertiary structures of a protein are destroyed but primary structure remains intact. C. Nucleotides are joined together by glycosidic linkage between $\mathrm{C}_{1}$ and $\mathrm{C}_{4}$ carbons of the pentose sugar. D. Quaternary structure of proteins represents overall folding of the polypeptide chain. Choose the correct answer from the options given below :
From the given following (A to D) cyclic structures, those which will not react with Tollen's reagent are : 
Given below are two statements: Statement I: Sucrose is dextrorotatory. However, sucrose upon hydrolysis gives a solution having mixture of products. This solution shows laevorotation. Statement II: Hydrolysis of sucrose gives glucose and fructose. Since the laevorotation of glucose is more than the dextrorotation of fructose, the resulting solution becomes laevorotatory. In the light of the above statements, choose the correct answer from the options given below
The number of possible tripeptides formed involving alanine (ala), glycine (gly) and valine (val), where no amino acid has been used more than once is:
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