The relative stability order of carbanions CH≡C-, CH₃ - and CH₂=CH^- is ____________

1. $\mathrm{CH}\equiv {\mathrm{C}}^{-}>{\mathrm{CH}}_2={\mathrm{CH}}^{-}>{\mathrm{CH}}_3^{-}$

2. ${\mathrm{CH}}_3^{-}>{\mathrm{CH}}_2={\mathrm{CH}}^{-}>\mathrm{CH}\equiv {\mathrm{C}}^{-}$

3. $\mathrm{CH}\equiv {\mathrm{C}}^{-}<{\mathrm{CH}}_2={\mathrm{CH}}^{-}>{\mathrm{CH}}_3^{-}$

4. ${\mathrm{CH}}_2={\mathrm{CH}}^{-}<\mathrm{CH}\equiv {\mathrm{C}}^{-}<{\mathrm{CH}}_3^{-}$

A solution of (+)-1 chloro-1-phenylethane in toluene racemizes slowly in the presence of small amount of SbCl₅ due to formation of

1. carbanion           2. carbene

3. free radical          4. carbocation

Which of the following is the most stable carbocation

1. 

2. 

3. ${\mathrm{CH}}_2=\mathrm{CH}-\stackrel{\oplus }{\mathrm{C}}{\mathrm{H}}_2$

4. ${\mathrm{CH}}_2=\stackrel{\oplus }{\mathrm{C}}\mathrm{H}$

Which of the following happens to be the carbanion with highest stability?

Which of the following carbocations is expected to be most stable?

1. 
2. 
3.  
4.