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I need help with number 10 part B. Which was the formula?
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- (CH3)3CCH=CHCl (1)NaNH2 -----> (2)H2O Which of the following is the product for the given reaction? a) (CH3)3CCH≡CH b) (CH3)3CCH=CH2 c) (CH3)3CCH=CHOH d) (CH3)3CCH=CHNH2reactions and products for C9H8O4 C9H8O4 + O2 --> C9H8O4 + H2O --> C9H8O4 + HCl --> C9H8O4 + OH- --> C9H8O4 + Na --> C9H8O4 + F -->Cyclohexene plus 1) Hg(OAc)2, H2O; 2) NaBH4; yields __________. HO2CCH2CH2CH2CH2CO2H a cyclic diketone cyclohexyne cyclohexanol OHCCH2CH2CH2CH2CHO
- Draw all products of the reaction of (1S,2R)-1-bromo-1,2-dimethylcyclohexane in 80%H2O/20%CH3CH2OHat room temperature..3. What is the main product for each of the following reactions? (a) p-Methylanisole + CH3CH2COCl, AlCl3 --------> ? (b) Toluene + Br2, light, then CH3CH2COCl, AlCl3 --------> ? (c) Acetophenone + CH3CH2Cl, AlCl3, then Br2, Fe -----> ? (d) Styrene + CH3CH2COCl AlCl3, then Br2, Fe -----> ? (e) Benzene + 1-chloro-2,2-dimethylpropane, AlCl3 -----> ? (f) Benzene + HCOCl, AlCl3 then 1-chlorobutane, AlCl3 -----> ? 4. Using arrows to show electron movement, write the stepwise mechanism for the major products in the reactions (3a and 3f) listed above.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!).
- For each compound, give the product(s) expected from (1) HgSO4>H2SO4@catalyzedhydration and (2) hydroboration–oxidation.(a) hex-1-yne (b) hex-2-yne(c) hex-3-yne32. Which of the following is INCORRECT? A. CH3COOH H+ + CH3COO- B. HF H+ + F- C. H2O H+ + O2- D. C2HO4- H+ + C2O42-N(CH2CH3)3 + HNO3 --------> a.) rewrite the reaction using bond-line structure of reagents and products of the reaction b.) supply the curved arrows explaining the mechanism of the reaction
- Bicyclo[2.2.1]heptan-7-one + PCC (in CH₂Cl₂) => A.) Bicyclo[2.2.1]heptan-7-ol B.) Bicyclo[2.2.1]heptanoic acid C.) Cyclohexanecarbaldehyde D.) All the given choices are possible products E.) No reaction(1R, 2S)-1-iodo-2-methylcyclohexane with boiling water? 1. Predict the products 2. Give the correct mechanism via correct arrow pushing, and arrow formalisms 3. Name each mechanism 4. Name each MAJOR and MINOR productsTreatment of 3-methylcyclohexene with HCl yields two products, 1-chloro-3methylcyclohexane and 1-chloro-1-methylcyclohexane. Draw a mechanism to explain this result.