Answer
Answer: (B) F. Wohler
Answer
Answer: (C) Carbon
Answer
Answer: (C) Tetrahedral
Answer
Answer: (C) 50%
Answer
Answer: (B) 3 sigma, 2 pi
Answer
Answer: (C) Not shown
Answer
Answer: (C) A bond projecting out of the plane towards the observer
Answer
Answer: (B) Acyclic or aliphatic compounds
Answer
Answer: (D) Heterocyclic
Answer
Answer: (B) -CH2
Answer
Answer: (D) -COOH
Answer
Answer: (C) Anisole
Answer
Answer: (C) Metamerism
Answer
Answer: (B) Carbocations and carbanions
Answer
Answer: (D) Tertiary carbocation
Answer
Answer: (B) sp2 hybridised
Answer
Answer: (C) Half-headed (fish hook) curved arrow
Answer
Answer: (A) Nucleophile
Answer
Answer: (C) BF3
Answer
Answer: (D) Inductive effect
Answer
Answer: (C) -NO2
Answer
Answer: (C) 139 pm
Answer
Answer: (B) Electromeric effect
Answer
Answer: (A) Hyperconjugation
Answer
Answer: (D) Sublimation
Answer
Answer: (C) Solubilities
Answer
Answer: (B) Fractional distillation
Answer
Answer: (C) Decompose at or below their boiling points
Answer
Answer: (C) Steam distillation
Answer
Answer: (A) Steam distillation
Answer
Answer: (B) Partition chromatography
Answer
Answer: (A) Partition chromatography
Answer
Answer: (C) Solvent from base line
Answer
Answer: (C) Sodium metal
Answer
Answer: (B) Prussian blue
Answer
Answer: (B) Blood red
Answer
Answer: (C) Iodine
Answer
Answer: (C) Ammonium molybdate
Answer
Answer: (A) Copper(II) oxide
Answer
Answer: (B) Potassium hydroxide
Answer
Answer: (C) Ammonium sulphate
Answer
Answer: (C) Nitro and azo groups
Answer
Answer: (B) Halogens and Sulphur
Answer
Answer: (C) Barium sulphate
Answer
Answer: (B) Iodine pentoxide
Answer
Answer: (B) Inductive effect
Answer
Answer: (C) sp3
Answer
Answer: (C) Neopentyl
Answer
Answer: (B) Isobutane
Answer
Answer: (C) Position isomers