In NBS reaction, Allylic Halogenation takes place. It is a radical Halogenation. NBS - N-Bromo Succinimide.
Allylic Halogenation takes place which is because of higher stability of Allyl radicals. Outside ring the Allylic position doesn't have a Hydrogen.
Answer: Option B
In acid- base Equilibrium reaction, The alcohols are more acidic than a secondary amine. Therefore Backward reaction is more favourable than forward reaction.
Answer: Option C.
NBS Rxn Which one of the following is a major product of the reaction? Br Br...
Which of the following represent all of the products of the following reaction? NBS hv ? Br Br Br Br Br Br А B с D m F OB,D,F Ο Ο А, В AD B,C,D,F O A,B,D,F O A,B,E Which of the products in question 19 would be considered the "thermodynamic" product? B חד E D ОА Ос
Most Upfield Protons (FE) The protons bonded to carbon spectrum. will appear the most upfield in the IH NMR a b OH Br O Аа O Bb с c D Unanswered Save
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Will rate! NaOH H2O 0 What is the major product of the above reaction? What is the major product of the following reaction? HgSO4 H,SO4, H,0 он В о он о Ос B ОА. 요 NaOH H2O What is the major product of the above reaction? 01 0-7 What is the best method to synthesize the above compound? Br2 CI AICI: FeBra CI Br, NH NH2 NBS KOBu AlCl3 Febrg KOH hv Br2 CL NH NH2 NBS KOBU" FeBr AICI,...
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H10.17 - Level 1 Homework. Unanswered What is the major product for the following reaction? Br NaOCH2CH3 Product CH3CH2OH CH3 CH3 OCH2CH3 OCH2CH3 CH3 O A A 0 BB [] Fullscreen o cc o C C o DD Ο Ε Ε Hint Note that the E2 reaction requires the B-proton to be anti-coplanar to the leaving group. In ring systems, this can only occur if the leaving group and the proton and the leaving group are on opposite sides of...
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