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Why is Bromobenzene unreactive under both SN1 and SN2 conditions?

Why is Bromobenzene unreactive under both SN1 and SN2 conditions?

Bromobenzene is unreactive in both SN1 and SN2 conditions. The carbon-bromine bond is very strong and even though bromine is the better leaving group it will not leave the aromatic ring; plus phenyl carbocations are very unstable.

Why is SN1 faster than Sn2?

For SN2, The Rate Of Reaction Increases Going From Tertiary To Secondary To Primary Alkyl Halides. For SN1 The Trend Is The Opposite. For the SN2, since steric hindrance increases as we go from primary to secondary to tertiary, the rate of reaction proceeds from primary (fastest) > secondary >> tertiary (slowest).

What makes an Sn2 reaction go faster?

SN2 indicates a substitution reaction that takes place in one step. A primary alcohol is preferred to prevent steric congestion caused by the simultaneous binding of the nucleophile and release of the leaving group. This reaction mechanism is faster because it omits the formation of a carbocation intermediate.

Is SN2 a two step reaction?

Bimolecular: A bimolecular reaction is one whose rate depends on the concentrations of two of its reactants. In bimolecular reactions, therefore, the slow step involves two reactants. For SN2 reactions, there are only two reactants; this means that the slow step is the only step.

Does Sn1 or SN2 have an intermediate?

An Sn2 and Sn1 reaction mechanism. Sn2 reactions are bimolecular in rate of reaction and have a concerted mechanism. On the other hand, Sn1 reactions are unimolecular in rate of reaction and have a step-wise mechanism. This process first involves bond cleavage by the LG to generate a carbocation intermediate.

What is the mechanism of SN2 reaction?

The SN2 reaction – A Nucleophilic Substitution in which the Rate Determining Step involves 2 components. -SN2 reactions are bimolecular with simultaneous bond-making and bond-breaking steps. -SN2 reactions do not proceed via an intermediate. -SN2 reactions give inversion of stereochemistry at the reaction centre.