The increasing order of +ve I-effect shown by H, CH₃, C₂H₅ and C₃H₇ is-

1. H < CH₃ < C₂H₅ < C₃H₇

2. H> CH₃ <C₂H₅ > C₃H₇

3. H < C₂H₅ < CH₃ <C₃H₇

4. None of the above

The effect that can explain the given order of acidity of the carboxylic acids is-

Cl₃CCOOH > Cl₂CHCOOH > ClCH₂COOH

1. +I effect

2. -I effect

3. +E effect

4. -E effect

${\mathrm{O}}_2{\mathrm{NCH}}_2{\mathrm{CH}}_2{\mathrm{O}}^{-}$ is more stable than ${\mathrm{CH}}_3{\mathrm{CH}}_2{\mathrm{O}}^{-}$ because :

The effect that makes 2,3–dimethyl-2-butene more stable than 2-butene is-

1. Resonance

2. Hyperconjugation

3. Steric effect

4. Inductive effect

Among the following groups maximum –I effect is exerted by:

\(1 . - C_{6} H_{5}\)
\(2 .\) \(- \left(OCH\right)_{3}\)
\(3 .\) \(- Cl\)
\(4 .\) \(-NO_2\)

The most stable carbocation among the following is-
1. \(({CH_3})_3C\overset{+}{C}H_2\)
2. \(({CH_3})_3\overset{+}{C}\)
3. \({CH_3}CH_2\overset{+}{C}H_2\)
4. \(({CH_3})\overset{+}{C}HCH_2CH_3\)

The most stable carbocation among the following is-

The most stable carboxylate ion among the following is-

1. ${\mathrm{CH}}_3-\stackrel{\mathrm{O}}{\stackrel{\left|\right|}{\mathrm{C}}}-{\mathrm{O}}^{-}$

2. $\mathrm{Cl}-{\mathrm{CH}}_2-\stackrel{\mathrm{O}}{\stackrel{\left|\right|}{\mathrm{C}}}-{\mathrm{O}}^{-}$

3. $\mathrm{F}-{\mathrm{CH}}_2-\stackrel{\mathrm{O}}{\stackrel{\left|\right|}{\mathrm{C}}}-{\mathrm{O}}^{-}$

4. ${\left(\mathrm{F}\right)}_2-\mathrm{CH}-\stackrel{\mathrm{O}}{\stackrel{\left|\right|}{\mathrm{C}}}-{\mathrm{O}}^{-}$

Compare the stability of the two resonating structures given below and mark the correct option:

1. (I)  is more stable than (II)

2. (II) is more stable than (I)

3. (I) and (II) both have the same stability 

4. None of the above

The carbocation among the following that doesn't get stabilized by resonance is :

1.		2.
3.		4.