Why does product A form faster than product B? (three correct answers)KCI+KOHKOHКСІ+H₂OFASTERSLOWERH₂OBA In an unfavourable conformation of the starting material, A can form from a favourable transition stateBB can form from a more favourable transition state(C) The elimination reaction requires a trans-coplanar arrangement of a C-H and and a C-Cl bondDThe bulky tert-butyl group prefers an equatorial conformation

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Answered: Why does product A form faster than…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter17: Alcohols And Phenols

Section17.SE: Something Extra

Problem 32MP: The conversion of 3 alcohols into alkenes under acidic conditions involves two cationic...

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To preview image click here 3D/sahorse structure Ph Br Ph Newman projection Alkene Product For the following compound a) Draw the 3-D structure in the reactive conformation for a E2 elimination using wedge/dashed bonds to indicate stereochemistry. b) Draw a Newman projection in the reactive conformation for E2 elimination c) Give the alkene product obtained upon a E2 elimination using a non-bulky base.
The conversion of 3 alcohols into alkenes under acidic conditions involves two cationic intermediates. For each reaction, draw the complete mechanism using curved arrows.
Organic chemistry question help! Question attached b
Dehydration of 1,2,2-trimethylcyclohexanol with H2SO4 affords 1-tert-butylcyclopentene as a minor product. (a) Draw a stepwise mechanism that shows how this alkene is formed. (b) Draw other alkenes formed in this dehydration. At least one must contain a ve-membered ring.
9) Draw the conformer structure, Newman projection, before elimination and the elimination product of the following reaction: Br CH3ONA H
Starting from the wedge-and-dash structure below (sighting down the indicated bond), rotate the back carbon to provide the structure in the conformation that will be capable of an E2 elimination. R/S stereochemistry is graded. # O H3C H Drawing > CI ||||| H Atoms, Bonds and Rings Tap a node to see s
What would be the major product of the following reaction? O CH3 || C6H5C-CHCH3 + D20 A) B) C) D) E) O CD3 C6H5C-CHCH3 O CH3 1-1 C6H5C-CDCH3 O CH3 C6D5C-CDCH3 O CD3 | | C6H5C-CDCD3 OD - C6H5CDCHCH3 CH3 OD room temp. ?
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Draw the alkene that would react with the reagent given to account for the product formed. ? + H₂O ● You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. 8 H₂SO4 // CH3 CH3CHCCH3 OH CH3 ? [F Previous Email Instruct
Explain why pentane-2,4-dione forms two different alkylation products (A or B) when the number of equivalents of base is increased from one to two.
Can you show the mechenismim for both the major and minor product?
Draw the organic product that is expected to form when the following compound is oxidized under biological conditions. (M) CH3 M oxidation 2req SH reduction M M) • You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • If no reaction occurs, draw the organic starting material. (M) C. P. aste opy M) = 2req s 2req M) M) ts ChomDondlo

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