Find out the statements which are not true. Choose the correct answer from the options given below :
- A, D & E only
- A, C & D only
- B & D only
- B, D & E only
Answer
(3) B & D only
Solution
A. As per NCERT, a resonance structure with more covalent bonds and less separation of opposite charges is more stable. ⇒ True.
B. In the electromeric effect the π-electrons shift towards the atom to which the attacking reagent gets attached. With an electrophile this gives the +E effect; with a nucleophile, the π-electrons move away from the attacked atom (–E effect). The statement interchanges the two. ⇒ Not true.
C. The inductive effect makes bonds polar; this permanent polarity gives polar compounds their dipole moment and the strong dipole–dipole attractions behind their high melting and boiling points. ⇒ True.
D. More alkyl groups on the doubly bonded carbons ⇒ more hyperconjugation ⇒ more stable alkene ⇒ lower heat of hydrogenation (e.g. (CH3)2C=C(CH3)2 releases less heat than CH2=CH2). ⇒ Not true.
E. Greater s-character holds the lone pair closer to the nucleus ⇒ carbanion stability: sp > sp2 > sp3. ⇒ True.
∴ Statements B and D are not true.
Answer: (3)