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Nilanjan Bhowmick AIR 3, CSIR NET (Earth Science)
Dinesh khalmaniya 1
The inductive (I) effect and the resonance (R) effect are the two ways in which substituents can donate or withdraw electrons from benzene ring. Inductive effect : The electron donating groups like -CH3, which is less electronegative than the ring activate the ring and direct the coming groups to orthodontist and para position. This is +I effect. The electron withdrawing groups like the halogen atoms which are more electronegative deactivate the ring and direct the coming groups to the meta position. This is -I effect. Resonance effect : The groups or atoms that have unbonded electrons i.e. lone pair of electrons on them, donate their electrons in the ring and they get delocalised. This is +R effect and it directs the coming groups to the ortho and para positions. E.g. NH3, CO groups The electron withdrawing groups pull the electron density towards themselves and the delocalisation of charge is reduced. This is -R effect and it directs the coming groups to the meta position. E.g the nitro group. Hope I answered your doubts correctly.
here at meta how can u say that - I -r exist
yha phenoxide ion k sence me ortho he to shi. apn acidiy OH group or cooH group k sence me dekhte he na so jo group inke ortho or para pr present hota vo group OH or COOH pr jada effect dalega na
mujhe bhot confusion ho ri hai samagh no aa rha