CORRECT order of stability for the following is

$\mathrm{CH}_2=\mathrm{CH}^{-}, \mathrm{CH}_3-\mathrm{CH}_2^{-}, \mathrm{CH} \equiv \mathrm{C}^{-}$

Given below are two statements :

Statement I : There are several conformers for n -butane. Out of those conformers,

Statement II : As the dihedral angle increases, torsional strain decreases from (X) to $(\mathrm{Y})$.

In the light of the above statements, choose the correct answer from the options given below

Find out the statements which are not true.

A. Resonating structures with more number of covalent bonds and lesser charge separation are more stable.

B. In electromeric effect, an unsaturated system shows +E effect with nucleophile and -E effect with electrophile.

C. Inductive effect is responsible for high melting point, boiling point and dipole moment of polar compounds.

D. The greater the number of alkyl groups attached to the doubly bonded carbon atoms, higher is the heat of hydrogenation.

E. Stability of carbanion increases with the increase in $\mathrm{s}-$ character of the carbon carrying the negative charge.

Choose the correct answer from the options given below :

$$ \text { Arrange the following carbanions in the decreasing order of stability. } $$

Choose the correct answer from the options given below :