Propose plauisible mechanisms of the the following reactions, including arrows to describe electron flow and all intermediates
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Propose plauisible mechanisms of the the following reactions, including arrows to describe electron flow and all...
20 3) Propose plausible mechanisms for two of the following four reactions, including arrows to describe electron flow and all intermediates. o CH,OH H2SO, H20 سلم NH b) crii DINH SOBE CN NH OH HN
3. Provide mechanisms to explain the following reactions. Show all key intermediates and indicat4e electron flow using arrows. осн CH,OH, H H od osty 4 Hoe om o Et d. CH,OH,H", (F980, H H cat. CF,SO3H -Et H2SO4 heat . a n n-1 Et nucleophiles EtOHOEt
provide mechanisms to explain the following reactions. Show all key intermediates and indicate electron flow using arrows. оСнз С. CH3ОН, н* Et OH H2SO4 b. Et heat
1) Provide structures for A-J in the following roadmap. H NaN LiAIH SOCI, CHINH + B с D- CH,OH (xs) CH,OH E+ A CHOS 1) KOH, H20 2) H,07 NH SOCI 2) Propose a mechanism for the following transformation, including arrows to describe electron flow, and all intermediates. CN Oro NaOH H2O are OH
2. Suggest reasonable mechanisms for each of the following reactions. Use curved arrows to show electron flow. (6) CH, + H2O HO (mixture of stereoisomers) -CH OH
Mechanisms. (2) For each experimental result shown below, propose a step-by-step "electron-pushing" mechanism, using "curly arrows". Show all intermediates (if there are any) explicitly. (a) HCI CI (b) н" +CH OH OCH, OH
1. Give stepwise mechanisms for the following reactions. Clearly show all intermediates and use arrows to show electron movement. - Hop Wow Peonic plure H-Br RO-OR, heat I Br b. R oh solla Red + S02 + Hl- c. Al cu. -CH = CH –O-CH3 Hbg, 4pH OH + HCl. 0 KOEI 1. Nat o Et, Etoh il I 10, EL + C CH₂ OH 2. Hoot TOE 1.HCl, H₂O 2. Et3N, Eto ce U
Write curved arrow mechanisms for TWO of the following reactions. CN CH NH2 1. LiAlH4 a) 2. H2O 3. OH CN COOH H2SO4/H20 b) heat
1) Provide structures for A-J in the following roadmap. H NaN CH,NH LAIRL CH,OH (XS) CH,OH SOCI, E A B D Fr, Cafe 1) KOH, HO 2) H0 NH, SOCI: 2) Propose a mechanism for the following transformation, including arrows to describe electron flow, and all intermediates. NaOH HO OH
General Organic Chemistry Homework I) Draw mechanisms and products for the following SN2 reactions. Use arrows to show electron movement. The reaction of 1-bromobutane with: a) OH- b) CH,CH2OK Na d) e) NH