Answered: 6) The compound shown is an… | bartleby

Organic Chemistry: A Guided Inquiry

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter24: Carboxylic Acids & Derivatives

Section: Chapter Questions

Problem 16CTQ

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6) The compound shown is an intermediate in a Robinson annulation reaction (product after Michael
reaction). Please provide the final Robinson annulation product and expected mechanism. Please show
all intermediates and use arrows to show the movement of electrons. (
NaOH, H₂O
Heat

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Remaining Time: 38 minutes, 42 seconds. Question Completion Status: 2 50 100 110 120 130 14 15 36 37 38 39 40 41 42 430 44 45 46 47 48 49 50 QUESTION 1 What is the rate-determining step in the following reaction? CH3 heat CH3 -CHCH3 HBr CH3 OH O Rearrangement of a secondary carbocation into a tertiary carbocation O Formation of secondary carbocation O Formation of primary carbocation - There is no rate-determining step because the reaction is concerted Formation of tertiary carbocation ESTION 2 re and Submit to save and submit. Click Save All Answers to save all answers. F1 20 F2 F3 F4 2# %24 2 3
is this an E1 or E2 mechanism for this reaction? What is the major product and step by step mechanism?

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