Explain the reasons for the changes in reactivity of Phenol, Benzene and MethylBenzene

The changes in reactivity are due to the electron donating/withdrawing properties of the substituted groups. For example the OH group in Phenol is electron donating. This means the electron density of the delocalised ring will have increased, meaning it can polarise bonds more readily. MethylBenzene is less reactive as the Methyl group is electron withdrawing, this means the electron density of the delocalised ring will have decreased, hence decreasing the reactivity. This makes it less reactive than Benzene.

AD

Related Chemistry A Level answers

All answers ▸

The Haber process is used to produce ammonia. (Insert equation here) Explain the optimum conditions for this reaction and why these may differ from the conditions used in industry.


Define ferromagnetism, paramagnetism and diamagnetism, and determine whether the following complexes a) AgCl b) [Fe(CN)6]4- c) [Mn(CN)6]4- d) Co(H2O)6Cl2 are ferromagnetic, diamagnetic or paramagnetic giving a full justification for your reasoning.


Draw an example using a diagram of Carbon, three "Y" substrates and an "L" indicating any leaving group the Sn1 nucleophilic substitution reaction. (3 marks) Which step is fastest (1 mark).


Explain how a hydroxynitrile is produced from a ketone