Question

Question 2 4 pts E1 and Sn1 reactions can compete. Check all of the reasons why E1 predominates in this week's reaction. Note: this question is graded by Canvas as "right minus wrong", subtracting points for wrong answers. o no good nucleophile is present in solution the E1 product is distilled out of the reaction mixture as it is formed, thus the reaction is driven to completion (Le Chatelier's Principle) the intermediate carbocation is too sterically hindered for substitution to occur the nucleophile is too bulky for substitution to occur

Answer 1

Ans: - The Reaction is write here is probably Ambercyot 15 in Exchange Resin. since the Ambercyot is an ion exchange resin. it is acidic in the nature. it is provides a non- nucleophili's mediom that booms dehydrated products, Hence the corect options are a&b ie ② no good nucleophile is present in solution The E, product is © distilled & the reaction as mixture it is the formed, thus reaction is doiven to completion (Le chatelies principle)