Give mechanism? CH CICH2CH20 catalyst 11-8, Scheme 10.11 PhCCO2CH3 cat 11-8 CICH2CH2O CO2CH3 75%, 98% e...
6. Given the following scheme: Ho gibalubong Ph;P=CH, toluene Grubb's Cat. OTBS a) Show the transition state and product for the transformation leading to product A. A b) Show each transformation and the product B for the reaction using the Grubb's catalyst:
8.(12 pts) Draw the mechanism for the addition of water to the alkene (with acid catalyst) Clearly show the 3-D geometry of the intermediate and be sure to clearly depict (in 3-D) all possible stereoismers that are produced. CH3CH2 H H2SO4 + H2O -CH₃ CHE
7) Give the mechanism including the transition state. сн.ct çı SN2 НН 8) Give the mechanism. CH1 보 SN1 CHCH,CH-C CH. но H Br 9) Give the mechanism of the reaction shown below. CH CI E1 CH,OH 10) When 1-bromo-2,2-dimethylcyclopentane is heated in ethanol, one of the products which results is shown below. Provide a detailed, stepwise mechanism for the production of this compound, and give the name of the mechanism by which it is produced. CH3 CH3
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you show me the mechanism steps please
1) о (2) CH SCH, (3) НA (cat.) НО LOH оро на сензор ОН W 1: 11 HOOCH CHCH (ә) С ен о. НО
CH, 7. Give the mechanism of following reactions (10") CH; CH CH,0 H- CH=CH-BT HỌC -CH-CH, + HgC-C=CHCH CHOH ī CHS OCH (1) 1) BrMg(CH2)MgBr.THF OH (2) 2)H30 8. Give the possible synthesis method of following compounds (29) CHE сн.
Please show mechanism
8) Give the major product of the following reaction. 8) 1. CHCH CHCH CH CHCH2CH CH,CH CHz HCH CH-CH3 CH.CHs D) CHCH.CH2 CHCH CH.CHi Ct CH2 0 CH2 CH3
Give the approximate equivalents 1. 2.24 liters, (s) . mL(s) mgls) 4. 75 mcg'smgls) 5. 98 mcg's 6. 10 oz- mL(s) 7. 208 lbs kg(s) mg(s) 8. 548 t(s) 9. 75 ml Kg(s) 10. 3 8 Write the meaning of the following abbreviations or symbols 6. amp 1. KVo 7. Anterior chest wall 2. tid 8. Stat 3. h 4. LA 10. As needed 5. elix
СО cat. H + NH2CH3 + H2CO2C CO2CH3 CO CHE Cocaine has been prepared by a sequence beginning with a Mannich reaction between dimethyl acetonedicarboxylate, methylamine, and butanedial. The mechanism involves the following steps: 1. Following initial protonation of the carbonyl oxygen, nucleophilic attack by the amine forms carbinolamine 1; 2. Proton transfer and elimination of water forms iminium ion 2; he enol form of the dicarboxylate ester attacks the iminium ion to form adduct 3; 4. Adduct 3 tautomerizes...
Give the structure of the major organic product, reactant, or
catalyst in each incomplete equation.
(e to i) please thanks!
CHE R ethylcyclohexane HCl Naoh CH,OH, Et, Y CH14) (an isomer of Y) Hg (0Ac), Nabtle H2SO4 (8) "3,3-dimethyl-1-butene 44. THE KOH ale, a НІ Et, o (h) 1.3 ACETONE 2.2nº (the only product!) (HOA) (an isomer of D I (C6H12) NaHSO4 + ACETONE 1. Ha (Ach, ng 2. NaBHA, THE II (C8H14) 1. O 2.Z, HOA (an isomer of...
Give a detailed mechanism for this reaction and give a separation
scheme
NUCLEOPHILIC ACYL SUBSTITUTION: Synthesis of an Ester Isoamyl acetate (Banana Oil) Purpose This experiment demonstrat and alcohol. The technique of refluxing the reaction mixture is introduced. es the procedure for the synthesis of an ester from a carboxylic acid Esters are an important functional group in organic chemistry, and esters are found widely distributed in nature. Many lower molecular weight esters are associated with natural fuit flavors and...