Q.10 Water can dissolve many organic molecules due to 1. Dipolar character and ability to form hydrogen bond 2. Hydrophilic character and high conductance 3. Amphiphilic character and high insultation capacity 4. Hydrophobic character and ability to fonn disulfide bond

Q.10 Water can dissolve many organic molecules due to
1. Dipolar character and ability to form hydrogen bond
2. Hydrophilic character and high conductance
3. Amphiphilic character and high insultation capacity
4. Hydrophobic character and ability to fonn disulfide bond

Correct Answer: Option 1

Water dissolves many organic molecules primarily due to its dipolar nature and hydrogen bonding capacity, which interact with polar functional groups like -OH and -NH₂ in solutes such as alcohols, sugars, and amines.

Option Analysis

Option 1: Correct

Water’s polarity (bent molecule, partial charges on O/H) enables dipole-dipole interactions and hydrogen bonding with organic molecules bearing electronegative atoms (O, N). This solvation shell stabilizes polar solutes like glucose or ethanol, overcoming lattice energy.

Option 2: Incorrect

Hydrophilic character describes water-loving solutes, not water itself; high conductance relates to ions (e.g., salts), irrelevant for neutral organics like methanol, which dissolve via H-bonding without conductivity.

Option 3: Incorrect

Amphiphilic refers to dual hydrophilic/hydrophobic molecules (e.g., surfactants); water lacks this and has no notable insulation capacity—it’s a conductor for ions.

Option 4: Incorrect

Hydrophobic means water-repelling, opposite of water’s solvent role; disulfide bonds (-S-S-) form in proteins via cysteine oxidation, unrelated to solubility.

Introduction to Water Solubility

Water can dissolve many organic molecules due to its dipolar character and ability to form hydrogen bonds, a core concept in biochemistry for exams like GATE Life Sciences. This property explains why polar organics like ethanol mix freely while hydrocarbons do not.

Key Solubility Mechanism

Water’s dipole (μ ≈ 1.85 D) and H-bonding (as donor/acceptor) surround polar groups, e.g., -OH in glucose forms multiple H-bonds.

  • “Like dissolves like”: Polar organics soluble up to ~4-5 C atoms per polar group.

  • Examples: Methanol (infinite solubility), butanol (limited).

Solubility Rules Comparison

Property Water’s Role Effect on Organics
Dipolar/H-bonding Solvation shell High solubility (alcohols, amines)
Hydrophilic Solute trait Not water’s property
Amphiphilic Surfactants Forms micelles, not dissolution
Hydrophobic Hydrocarbons Insoluble (e.g., hexane)

This confirms option 1 as the correct reason water dissolves organic molecules.

Exam Tips for Life Sciences

Memorize: H-bonding > chain length for solubility. Avoid traps like conductance (ionic) or disulfides (covalent). Practice with glucose vs. cholesterol.

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