Here's the explanation:
1. Understanding Osmosis:
Osmosis is the natural movement of water molecules from a region of higher water concentration (lower solute concentration) to a region of lower water concentration (higher solute concentration) through a semi-permeable membrane. This process aims to equalize water concentrations on both sides of the membrane.
2. Reverse Osmosis:
Reverse osmosis is the opposite process where water is forced to move from an area of lower water concentration to higher water concentration, requiring the application of external pressure.
3. Analyzing the Mango Scenario:
When an unripe mango is placed in a concentrated salt solution:
4. Process Identification:
Since this involves the natural movement of water from high to low concentration areas without external pressure, it is regular osmosis, not reverse osmosis.
Conclusion:
The correct explanation is that the mango loses water due to osmosis.
Final Answer:
The correct answer is (D) it loses water due to osmosis.
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.