Let's analyze each statement:
A) It is an aldohexose:
This is true. Glucose is a six-carbon sugar (hexose) with an aldehyde functional group (aldo-).
B) On heating with HI it forms n-hexane:
This is also true. HI is a strong reducing agent that removes all oxygen atoms from glucose, reducing it to n-hexane.
C) It exists in furanose form:
This is partially true but misleading. While glucose can exist in both pyranose (six-membered ring) and furanose (five-membered ring) forms, the pyranose form is overwhelmingly predominant in solution. The furanose form exists only in minor amounts.
D) It does not give Schiff's test:
This is false. Glucose does give Schiff's test because its open-chain form contains an aldehyde group (in equilibrium with cyclic forms). Schiff's reagent reacts with aldehydes to produce a pink-magenta color.
Conclusion:
While statements A, B, and C have elements of truth, statement D is completely incorrect. The statement that is not true is (D).
Final Answer:
The incorrect statement is (D).
Write IUPAC names of the following compounds and classify them into primary, secondary and tertiary amines.
(i) (CH3 )2CHNH2 (ii) CH3 (CH2 )2NH2 (iii) CH3NHCH(CH3 )2
(iv) (CH3 )3CNH2 (v) C6H5NHCH3 (vi) (CH3CH2 )2NCH3 (vii) m–BrC6H4NH2
Give one chemical test to distinguish between the following pairs of compounds.
(i) Methylamine and dimethylamine
(ii) Secondary and tertiary amines
(iii) Ethylamine and aniline
(iv) Aniline and benzylamine
(v) Aniline and N-methylaniline
Account for the following:
(i) pKb of aniline is more than that of methylamine.
(ii) Ethylamine is soluble in water whereas aniline is not.
(iii) Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.
(iv) Although amino group is o– and p– directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.
(v) Aniline does not undergo Friedel-Crafts reaction.
(vi) Diazonium salts of aromatic amines are more stable than those of aliphatic amines. (vii) Gabriel phthalimide synthesis is preferred for synthesising primary amines.