14. Which of the following statements about nucleophilic substitution reactions is INCORRECT? (A) (B) ©), The rate of nucleophilic substitution reactions can be affected by the solvent. A Sy2 reaction always proceeds with complete inversion of stereochemistry at an asymmetric carbon at the reaetion centre. ‘An SyI reaction will be slow at a tertiary carbon due to steric hindrance. (D) A good leaving group is required for nucleophilic substitution reactions. 15, Several products are formed in this reaction: 16. ) ( HCI (aq) oo Which of the following compounds COULD NOT be formed. wy yy (A) (B) © (@) Which of the following statements about nucleophilic substitutions reactions is CORRECT? (A) An Sy2 mechanism always occurs in two steps. (B) A strong nucleophile is essential for a substitution via an Sy! mechanism. (C) An Sy2 reaction is stereospecific. (D) An Sy1 reaction will be slower in a more polar solvent.18 The products from the following mechanistic step are: © 0) 19. The products from the following mechanistic step are: wo? f HOH, a) pHs 1,0 CH HH OH, e ® +8F CH H CH: a8 oO Sys + H:0 + Br CHs 4 CH,Br - o > + HO CHs