Indicate the major product of the following reaction, drawing the intermediate products if any. H3CO 1° H-CHO, (piperidine) N 2° (CH3)2CuLi 3º H3O+
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- What is the rate law implied by the mechanism given below? CH3COCH3(aq) + H+(aq) ←→ CH3C(OH)CH3+(aq) (fast, reversible) CH3C(OH)CH3+(aq) → CH3C(OH)=CH2(aq) + H+(aq) (slow) CH3C(OH)=CH2(aq) + Br2(aq) → CH3C(OH)CH2Br+(aq) + Br-(aq) (fast) CH3C(OH)CH2Br+(aq) → CH3COCH2Br(aq) + H+(aq) (fast) A. Rate = k[CH3COCH3][H+] B. Rate = k[CH3COCH3] C. Rate = k[CH3COCH3][Br2] D. Rate = k[CH3COCH3]2 E. Rate = k[CH3COCH3][Br2]/[H+] (Answer is A, looking for explanation why!).Match the reactant with the product of its reaction with HClO4. Leave blank if there is no reaction. Group of answer choices K2S KHCO3 HNO3 K2SO3When mixing aniline and acetic acid together, which direction will be favored at equilibrium? C6H5NH2 (aq) + CH3COOH (aq) <--> C6H5NH3+ (aq) + CH3COO-1 (aq)
- Answer choices for each are the following: unimolecular reaction Br- acetone Cl- substitution reaction elimination reaction CH3OH CH3O- F-Present the concerted pathway of the reaction below. (2E)-hex-2-ene + H2 and PtRank the species in each group in order of increasing nucleophilicity. a. CH3CH2S−CH3CH2O−, CH3CO2− in CH3OH b. CH3NH2, CH3SH, CHOH in acetone c.−OH, F−, Cl− in acetone d. HS−, F−, Cl− in CH3OH
- Are the following nucleophiles, electrophiles, they be both a nucleophile or electrophile, or neither? pyridine alkenes Hg+ (ex. Hg(OAc)2 CH3ONa PBr3In this equilibrium reaction, what is the favored direction? forward, resverse, or equlibrim? CH3CH2CH(OH)CH2CH3 + Na-1CH2CH2CH3 <==>Draw the products of the following reactions. Use curved arrows to show where the pair of electrons starts and where it ends up. a. ZnCl2 + CH3OH b. FeBr3 + Br c. AlCl3 + Cl−
