Chix I a ether, o°c No Reaction hace, the reaction pathway should be Sv 2 (Substitution Nucleophilic kimolecular). But the backside attack by the Ir at the ca carbon centre does not take place since , I is a weaker Nucleophile compared to ci So, the c-cl bond being stronger than c-I bond, the formation of the latter
does not take place. The reaction temperatwee was 0°C, which means the reaction was performed under cold conditions. 7. M3 H2O ett Hill ont no ficha Be toc hont no cu na H; Here the reaction pathway is Snil Substitution Nicliophilic 'Unimolecular The reaction proceeds via formation of a zo stable carbocation (tertiary carbocation) and thus we get a mixture of products he pena "Св ha с ®/42°, Қхһим в @ + B y HC (3*Carbocatii *, why deые
chz Din Cuz COM ИВя. Ann Cuz t ko OH honum the reaction was performed at -5°C which means at lower temperature - the reaction takes place and it is exothermic in nahore 3. CH3 CH₂o els ner Br CH₂ CN, -10% ochz Here, the reaction proceeds via Sn2 pathway. The clzo attack from the backside at the chiral cakebon centre and the c-Br bond breaks leading the formation of the product. The reeaction takes place - at very low temperature i.e. it is highly exothorchia in nahure. ochz Coena, دام می وما ما