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8.36 Identify which of the following methods is more efficient for producing 3,3-dimethy cyclohexene. Explain your...
32. Identify which of the reactions W-Z would synthesize 3,3-dimethylcyclopentene most efficiently. Then explain why the other routes would be less efficient. OH H2SO4, H,O heat 3,3-dimethylcyclopentene KOC(CH3)3 KOC(CH3)3 H2SO4, H,0 heat
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
help with all of these ! Question 8: Which is the better retrosynthesis for the given target molecule? Explain and provide a one-step synthesis of the target molecule. Br Br Hас Hас Hас .CH3 b) NaQH CHy Question 7: Draw the plausible mechanism for each of the folllowing transformations: a) CHy Не нс CHs CH СH, CH3 conc. H,SO -CH3 heat CH он Question 5 Predict the major and minor products for the following reactions: a) NaSH Н,с b) Br...
CHEM 330 Homework # 9 Name: Due: 11/06/19 Identify which of the following two reactions you would expect to occur more rapidly and then explain your choice. (2 pts) 4. НЕг HЕг 5. Suggest an efficient target synthesis for the following transformation. (3 pts) OH 2 steps Br Provide the complete mechanism for the following reaction. (6 pts) 6 но HаРОд Н-о
Please QUANTITATIVELY (ie. by how much) identify which is the stronger nucleophile, and EXPLAIN why it is better. Use this table to correlate the peaks in the GC printouts to product identification. Then use the table entries for area or area% in the GC results to calculate ratios. The Nucleophilic Medium contains: RT (min) Compound RT (min) Compound 2.06 1-butanol 2.34 1-chlorobutane 1.35 2-methyl-2-propanol 3.04 1-bromobutane 1.68 2-chloro-2-methylpropane 1.75 2-butanol 2.14 2-bromo-2-methylpropane 2.09 2-chlorobutane 2.70 2-bromobutane Note: Deviations for RT...
Consider the following reaction NaOEt ------>EtOH a) Identify the mechanism(s) by which the reaction will occur. If there is more than one mechanism that can operate, identify the mechanism that will predominate. Explain your reasoning clearly. b) Predict all possible product(s) that will be formed and identify them as major and minor products.
please explain 3. Predict which of the following compounds is more acidic, and explain your choice. (6 pts) -NH2 -NH2
1. For each pair of compounds identify which compound can be more readily deprotonated and explain your choice. (a) 2,4-dimethyl-3,5-heptanedione or 4,4-dimethyl-3,5-heptanedione (b) acetophenone or benzaldehyde 2. Predict the major product for the following transformation and propose a mechanism for its formation. 1. H307, Br2 2. Base C6H100
Identify which of the following two reactions you would expect to occur more rapid Addition of HBr to 2-methylpent-2-ene or Addition of HBr to 4-methylpenl-1-ene. Explain your choice clearly.
Please explain your answer Which of the following reactions is NOT an isodesmic reaction? Н,с-он "сн, CH4 + Hас -Он (А) + (В) ОН + ОН CI н н Н н н Br Br Br (C) + Br Br н Н Br Н Н (D) з СH4 2 Hа Select one: а. А b. В С. С d. D вооо