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- Predict the mechanimsm and reactants to synthesize the picture below. Write legibly and ill give you a thumbs up.After E2 elimination, will the following molecule contain deuterium? Why or why not?Can you draw the products that form when 1-butene reacts with; O3, then Me2S OsO4, then NaHSO3/H2O Br2 in H2O Please analyze in detail for each. Also can you please reply fastly?
- i need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,One of the heptanedione isomers below has a pka of approximately 9 rather than 20. Which isomer? Why? Draw its conjugate base and offer a full explanation of its acidity.Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?
- Minor product via E1 for 2-butanol and HCl?Your task is to synthesize trans-1, 2-cyclohexanediol, beginning with cyclohexene. What reagent(s) will accomplish this task in good yield? Group of answer choices cold aqueous KMnO4 PCC, CH2C12, 0 oC excess dilute aqueous acid (H2O /H +1) MCPBA followed by dilute aqueous acid (H2O / H+1) Please answer fast i give you upvote.EFFECTS OF SUBSTITUENTS ON ELECTROPHILIC AROMATIC SUBSTITUTIONA halogen group (-X) is deactivating, what place would it occupy on the following scale? –NO2 > –CN > –SO3H > –CHO > –COR > –COOH > –COOR > –CONH2 > –CCl3 more deactivating less deactivating
- Could you please show me how to draw in the electron arrows to account for the following mechanistic step. Solve it asapCan you please check my work on the following ochem reaction scheme and let me know if it is correct or what is wrong... the question was: Consider 3,4-dimethylpiperidine being subjected to the following: Step 1: CH3I (excess); Step 2: NaOH, heat Step 3: CH3I (excess); Step 4: NaOH, heat Provide the bond line structures for the major organic product obtained in each step and discuss the regiochemistry for Step 2.Can someone explain the answers to 28, 29, and 30? The answers are B, A, A. I understand lindar catalyst makes cis alkenes and Na/NH3 makes trans alkenes but I dont understand how the second step of Br2, OsO4 influences the stereochemistry between the 2 . Will rate quickly if helpful. Thanks!