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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Organic chemistry question help! Question attached b
9) Draw the conformer structure, Newman projection, before elimination and the elimination product of the following reaction: Br CH3ONA H
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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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7oar tavorite distributel berzene derivatives You must have 2 molecules, Please Substituent Draw two of make ( deactivators) and the other substituent an one electron with drawin grave an electron donanting group (actiuators) Une of these molecules must have substituents meta tu each other. The other molecule must must Your molecule have substituents para to each other for each molecule respectively. substituent donathng One electron withd raving electron Substituent anel one contain
a) Draw the mechanism, using good curved arrow notation, for the reaction of 2-methyl-2- butene with bromine in water, omitting any stereochemistry: b) (R)-3-butyn-2-ol is treated with 2 mol of HBr, yielding optically active Compound A (C4H8OBr2). Draw the structure of the reaction with the correct stereochemistry. c) Name Compound A above, including stereochemistry. d) Compound A is treated with HBr to yield Compound B (C4H7Br3). The resulting solution is optically inactive. Draw the product(s) obtained and explain why there is a loss in optical activity.
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