Comparison of Nucleophilicity |Basicity #Shorts ||Organic Reaction Mechanism||NEET||JEE||CUET|NET

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#Basicity also explained on the basis of #nucleophilicity . All #nucleophile are Lewis bases; they donate a #lone pair of electrons. A base is just the name we give to a nucleophile when it’s forming a bond to a #proton .
Nucleophilicity depends on many factors, including charge, basicity, solvent, #polarizability and the nature of the substituents.
Carbon has least #electronegativity so CH3− will have highest nucleophilicity. therfore the correct order of nucleophilcity is CH3− NH2− HO− F−.
#Nucleophile means "nucleus loving" which describes the tendency of an #electron rich species to be attracted to the positive nuclear charge of an electron poor species, the electrophile . The nucleophilicity expresses the ability of the nucleophile to react in this fashion.
The nucleophilicity increases as you increase the basicity. So as you go across the #periodic table from right to left, nucleophilicity also increases.

Question on Nucleophilicity ||Basicity ||Organic Chemistry| Reaction Mechanism||NEET||JEE||CUET||NET
@BipChemTech #neet #bsc #cuet #jee #icar #organicchemistry #organic #reactions #reactionmechanism #reaction #reactive
#comparison of #nucleophilic
@BipChemTech #neet #bsc #cuet #jee #icar #organicchemistry #organic #reactions #reactionmechanism #reaction #reactive
#comparison of #nucleophilic
Comparison of Nucleophilicity |Basicity #Shorts ||Organic Reaction Mechanism||NEET||JEE||CUET|NET
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