Determine reagents C and D from the reaction scheme below. Choose two (2) answers. Select one or more: O Cl₂, H₂O OHCI ο Η2Ο, Δ Cl₂, CCl4 H₂SO. A OH C D
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- A student adds NBS to a solution of 1-methylcyclohexene and irradiates the mixture with a sunlamp until all the NBS has reacted. After a careful distillation, the product mixture contains two major products of formula C7H11Br. (a)Rank these three intermediates from most stable to least stable.Kk.174. Please fill out this reaction mechanism with the missing reagents and intermediate products with a complete arrow-pushing mechanism.Choose the best reagents from the list provided below for carrying out the following conversion. Match the reagent with the step number. HCl (aq), Zn(Hg) Br2, FeBr3 Na/NH3, -33 degrees C NBS, light KMnO4, H3O+ Mg metal, ether KOH, EtOH, heat
- Reaction of HBr with 2-methylpropene yields 2-bromo-2-methylpropane. What is the structure of the carbocation formed during the reaction? Show the mechanism of the reaction.3H. Put it all together. Predict the E1 products of the following reaction. Label alkenes as E/Z. 4. Predict the E1 products of the following reaction. Label akenes as E/Z.For each reaction, show the generation of the electrophile and predict the products.(a) benzene + cyclohexene + HF (b) tert@butyl alcohol + benzene + BF3
- Please give a detailed stepwise mechanism for the following reactions of Q.1 and Q.2. All arrows, charges, intermediates, and resonance structures must be shown.Draw the products, including their configurations, obtained from the reaction of 1-ethylcyclohexene with the following reagents:a. HBr b. H2, Pd/C c. R2BH/THF, followed by HO– , H2O2, H2O d. Br2/CH2Cl2For each reaction, show the generation of the electrophile and predict the products.(a) benzene + cyclohexene + HF (b) tert@butyl alcohol + benzene + BF3(c) tert@butylbenzene + 2@methylpropene + HF
- Propose a mechanism for each reaction, showing explicitly how the observed mixtures of products are formed. cyclopenta-1,3-diene + Br2 S 3,4-dibromocyclopent-1-ene + 3,5-dibromocyclopent-1-eneTreatment of cis-2-bromocyclohexanol with NaOH yields cyclohexanone instead of an epoxide. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism.Choose the best reagents from the list provided below for carrying out the following conversion. Match the reagent with the step number. HCl (aq), Zn(Hg) KMnO4, H3O+ CH3Cl, AlCl3 HNO3, H2SO4 Cl2, FeCl3 fuming sulfuric acid