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Although cholrine is electron withdrawing group.yet it is ortho nd para directing in electrophilic aromatic substitution reactants.why?
Solution) Halogens are an exception of the deactivating group that directs the ortho or para substitution.The halogens deactivating the ring by inductive effect not by the resonance even though they have an unpaired pair of electrons.The unpaired pair of electrons gets donated to the ring,but theinductive efffect pullles away the electrons from the ring by the elecronegitivity of the halogens.
write the structures of the major product (saytzeff elimination) when the following alcohols are dehydrated with hot,concentrated sulphuric acid. 1. 3-methyl-2-butanol 2. 2-pentano
reactivity of f-block elements
Electrons and nuclei The familiar planetary model of the atom was proposed by Rutherford in 1912 following experiments by Geiger and Marsden showing that all the mass of an
Define Interfacial potential differences? What is the source of an open-circuit, zero-current cell potential? When no electric current passes through the cell, the electric pot
Molecule in itself is electrically stable so it cant act as ligand So that it can acts as the negative and pasitive ligand.
Fe3+ + e ------> Fe2+
Aromaticity or aromatic character The characteristic behaviour of aromatic compounds is termed as aromaticity. Aromaticity is due to the extensive delocalisation of p-electron
explain vsepr thheory
use and purpose 0
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