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(a)
Interpretation:
The major product of the given reaction is to be predicted.
Concept introduction:
The synthesis of ester from
Methyl group <primary alkyl group <secondary alkyl group = aryl group <tertiary alkyl group < H.
(b)
Interpretation:
The major product of the given reaction is to be predicted
Concept introduction:
The synthesis of ester from ketone or aldehyde in presence of CF3CO3H and meta-chloroperbenzoic acid(MCPBA) is called Baeyer Villiger oxidation. In the Baeyer villiger oxidation oxygen atom from peroxide is inserted between the carbonyl carbon and one of the groups initially bonded to carbonyl carbon. If ketone is symmetric, only one product is formed, but if ketone or aldehyde is unsymmetric, the major product depends on which group leaves from carbonyl carbon. The ability of the leaving group is called migratory aptitude. The order of migratory aptitude is as follows:
Methyl group <primary alkyl group <secondary alkyl group = aryl group <tertiary alkyl group < H.
(c)
Interpretation:
The major product of given compound is to be predicted and reaction is shown as.
Concept introduction:
The synthesis of ester from ketone or aldehyde in presence of CF3CO3H and meta-chloroperbenzoic acid(MCPBA) is called Baeyer Villiger oxidation. In the Baeyer villiger oxidation oxygen atom from peroxide is inserted between the carbonyl carbon and one of the groups initially bonded to carbonyl carbon. If ketone is symmetric, only one product is formed, but if ketone or aldehyde is unsymmetric, the major product depends on which group leaves from carbonyl carbon. The ability of the leaving group is called migratory aptitude. The order of migratory aptitude is as follows:
Methyl group <primary alkyl group <secondary alkyl group = aryl group <tertiary alkyl group < H.
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Chapter 21 Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
- Draw all 8 stereoisomers, circling each pair of enantiomer(s)/ mirror image compound(s)arrow_forwardBookmarks Profiles Tab Window Help Chemical Formula - Aktiv Che X + → C 11 a app.aktiv.com Google Chrome isn't your default browser Set as default Question 12 of 16 Q Fri Feb 2 Verify it's you New Chrome availabl- Write the balanced molecular chemical equation for the reaction in aqueous solution for mercury(I) nitrate and chromium(VI) sulfate. If no reaction occurs, simply write only NR. Be sure to include the proper phases for all species within the reaction. 3 Hg(NO3)2(aq) + Cг2(SO4)3(aq) → 3 Hg₂SO (s) + 2 Cr(NO3), (aq) ean Ui mate co ence an climate bility inc ulnerabili women, main critic CLIMATE-INI ernational + 10 O 2 W FEB 1 + 4- 3- 2- 2 2 ( 3 4 NS 28 2 ty 56 + 2+ 3+ 4+ 7 8 9 0 5 (s) (1) Ch O 8 9 (g) (aq) Hg NR CI Cr x H₂O A 80 Q A DII A F2 F3 FA F5 F6 F7 F8 F9 #3 EA $ do 50 % 6 CO & 7 E R T Y U 8 ( 9 0 F10 34 F11 川 F12 Subr + delete 0 { P }arrow_forwardDeducing the reactants of a Diels-Alder reaction n the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? ? Δ • If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. • If your answer is no, check the box under the drawing area instead. Explanation Check Click and drag to start drawing a structure. >arrow_forward
- Predict the major products of the following organic reaction: + Some important notes: A ? • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Explanation Check Click and drag to start drawing a structure.arrow_forwardif the answer is no reaction than state that and please hand draw!arrow_forward"I have written solutions in text form, but I need experts to rewrite them in handwriting from A to Z, exactly as I have written, without any changes."arrow_forward
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