1. Tardigrade
  2. Question
  3. Chemistry
  4. SN reaction is given by these compounds, which have a nucleophilic group and a good leaving EWG. It should be stable after leaving with bonding pair of bare 's and it should have high polarisability Nucleophilic aliphatic substitution reaction is mainly of two types SN 1 and SN 2 ⋅ SN 1 mechanism is a two-step process. Reaction velocity of SN 1 depends only on the concentration of the substrate. It proceeds viathe formation of carbocation, optically active substrate gives ⊕ and ominus forms of the product In most of the cases, the product usually consists of 5-20 % inverted and (95-80 %) racemised species. The more stable is the carbocation, the greater is the proportion of racemisation. In solvolysis reaction, the more nucleophilic is the solvent, the greater is the proportion of inversion Which of the following will give SN reaction?

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Q. SN reaction is given by these compounds, which have a nucleophilic group and a good leaving EWG. It should be stable after leaving with bonding pair of $\bar{e}$ 's and it should have high polarisability
Nucleophilic aliphatic substitution reaction is mainly of two types $SN ^1$ and $SN ^2 \cdot SN _1$ mechanism is a two-step process. Reaction velocity of $SN ^1$ depends only on the concentration of the substrate. It proceeds viathe formation of carbocation, optically active substrate gives $\oplus$ and $\ominus$ forms of the product
In most of the cases, the product usually consists of $5-20 \%$ inverted and $(95-80\%)$ racemised species. The more stable is the carbocation, the greater is the proportion of racemisation. In solvolysis reaction, the more nucleophilic is the solvent, the greater is the proportion of inversion
Which of the following will give SN reaction?

Haloalkanes and Haloarenes

Solution:

All