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Phenylamine is a weaker base than ammonia. The lone pair on the nitrogen of phenylamine is delocalised into the ring, thus making the lone pair less available to combine with hydrogen ions. Also, in order...
Stage 1 -Bonding 1a) Each C has three (covalent) bonds 1b) Spare electrons (in a p orbital) overlap (to form a pi cloud) 1c) delocalisation Stage 2 -Shape 2a) Planar 2b) Hexagon/6 carbon ring/120o b...
The electron configuration is:{Ar]4s13d10Copper donates one of the electrons in its S orbital to the d orbital in order to make itself more stableCopper 2+ is [Ar]3d9The 4s electrons are lost first as the...
1s22s22p6
Electrophilic Substitution
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