We need at least 10 more requests to produce the answer.
0 / 10 have requested this problem solution
The more requests, the faster the answer.
16. draw a complete curved-brow mechanism kend predict the products 04 eltz b/ CH HON, KCN...
Draw a complete curved-arrow mechanism, and predict the products. HO CH3 ? HCN, KCN ? CH3
Draw a complete curved‐arrow mechanism, and predict the products. for both problems HO Сн, С. HCN, KCN CH3 ?
Draw complete curved arrow medachnisms and predict products. НО. CH3 с. O HCN, KCN CH3
5. Draw the major products of the following reactions: a) (S)-2-Iodopentane + KCN in methanol. b) 2-bromo-2-methylpropane + LIN(CH(CH,),), in THF. c) 2-Chloro-1-ethanol + potassium tert-butoxide (KO'Bu). d) Cis-2-methyl-1-chlorocyclohexane + methanol. e) Potassium tert-butoxide (KO'Bu) and methyl iodide in THF. f) Draw a detailed curved arrow pushing mechanism for reaction 5d above. Draw the reactants cis-2- methyl-1-chlorocyclohexane + methanol, and show each and every electron flow that converts them into the major products.
Draw the mechanism and predict the major product for each of the following reactions. (b) 0 la) 0 1. KCN, HO 2 2. H SO 1. KCN, HẠO. 2. 2. H,SO 1. CH MgBr, ether 2. H2O 2 (e) 0 2°Cull 2. H2O CH,CH SNa 2. Ethanol
Draw the curved arrow mechanism and predict the product(s) for the 1st step only. Your products will be charged.
a) complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. a) Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the Draw the structure of the organic product formed in the reaction. Draw lone pairs. conversion to the product. CH3CH2OH -CI...
5. Draw the major products of the following reactions: a) (S)-2-Iodopentane + KCN in methanol. b) 2-bromo-2-methylpropane + LiN(CH(CH3)2), in THF. c) 2-Chloro-1-ethanol + potassium tert-butoxide (KO-Bu). d) Cis-2-methyl-1-chlorocyclohexane + methanol. e) Potassium tert-butoxide (KO-Bu) and methyl iodide in THF. f) Draw a detailed curved arrow pushing mechanism for reaction 5d above. Draw the reactants cis-2- methyl-1-chlorocyclohexane + methanol, and show each and every electron flow that converts them into the major products.
(iii) Please predict the products and draw the mechanism for: 7.5 pts. H/CH OH 3
a) Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. CH3 :Ci: CH3CH2OH -Cl b) Select the option that describes the mechanism of the reaction above. O E1 O E2