Chemistry Question 17Why does product A form faster than product B? (three correct answers)KCI+H₂Oད་KOHKOHKCI+FASTERSLOWERH₂OBA) In an unfavourable conformation of the starting material, A can form from a favourable transition stateB B can form from a more favourable transition stateThe elimination reaction requires a trans-coplanar arrangement of a C-H and and a C-Cl bondThe bulky tert-butyl group prefers an equatorial conformationQuestion 18What happens when an alkene is treated with an aqueous solution of potassium permanganate?A No reaction will take place.B) It will form an alcohol.It will form an alkane.D It will form a diol.Question 19What is the stereoelectronic requirement for this reaction? (three correct answers)BrKOMe+ KBr + MeOH(A) Equatorial arrangement of a hydrogen and the leaving bromideⒷ trans-coplanar arrangement of a hydrogen and the leaving bromideAnti-periplanar arrangement of a hydrogen and the leaving bromideA conformation with the bromine axial

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Answered: Question 17 Why does product A form…

Organic Chemistry

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Chapter30: Orbitals And Organic Chemistry: Pericyclic Reactions

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Problem 14MP: Plastic photochromic sunglasses are based on the following reversible rearrangement of a dye inside...

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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.
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