Which one of c6h5cl and c6h5ch2cl will react easily with aqueous KOH?

Answer: The Chlorodiphenyl methane will Easily Hydrolyze by aqueous KOH. As we know, Stable compounds are Easy to Hydrolyze by KOH as compared to other compounds. Cholorodiphenyl methane is a secondary carbocation while Benzoyl Chloride is a primary Carbocation.

Which of the following can be most easily hydrolysed?

Alum and cyanamide can easily be hydrolyzed.

Which of the following is more easily hydrolysed by KOH?

CH3CHClCH2CH3 is more easily hydrolysed. This is so both the given compounds would majorly follow the SN1 mechanism, since a stable intermediate can be obtained. The intermediate obtained on hydrolysis of the first compound is more stable than the one obtained on hydrolysis of the second.

Which of the compound will react faster in SN1 reaction with OH ion CH3CH2Cl or C6H5CH2Cl?

CH3CH2Cl or C6H5CH2Cl. The rate of SN1 reaction depends upon the stability of carbocation intermediate formed during the reaction. Hence C6H5CH2Cl will react faster due to the resonance stabilisation of carbocation. While in CH3CH2Cl carbocation is stabilised only through hyperconjugation.

Which of the following is most easily hydrolysed with aqueous KOH solution?

If carbocation is stable, then the compound is easily hydrolyzed by aqueous KOH. In the given compounds benzyl chloride forms primary carbocation, while chlorodiphenylmethane forms secondary carbocation, which is more stable than primary carbocation, hence C6H5CHClC6H5 is more easily hydrolysed by aqueous KOH.

Which of the following is most easily hydrolysed sf6?

The answer is Tellurium Hexafluoride.

Which one of the following compounds is more easily hydrolyzed by KOH and why 2 chloro butane or Chloropropane?

Hydrolysis of 2-chloro butane by KOH will result in the formation of secondary carbocation as an intermediate and hydrolysis of chloropropane will result in the formation of primary carbocation.

Which of the following is easily hydrolysed CCl4?

Give reasons for the following:(a) CCl4 is immiscible in water, whereas SiCl4 is easily hydrolysed.

Which compound reacts most rapidly by SN1 reaction?

(C6H5)3CCl is hydrolysed most rapidly by SN1 because (C6H5)3C+ is most stable.

Which one is more easily hydrolysed and why?

Which of the following is easily hydrolysed TeF6?

However, TeF6 which is in the same group as Sulphur can undergo hydrolysis as Tellurium is much bigger in size and can provide enough space for incoming water molecules to donate its lone pair in the vacant d-orbitals. For the same reasons SiCl4can also get hydrolysed easily.