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A: #12: The balanced chemical equation is 2SO2(g) + O2(g) → 2SO3(g)
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A: Given , Reaction : 2OF2(g) →O2(g) +2F2(g) ∆H=-49.4 kJ
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- Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.The reaction of (S)-2-bromopentane with potassium cyanide to yield 2-methylpentanenitrile (2-cyanopentane) occurs via a nucleophilic substitution pathway. The reaction is 100% stereospecific.Provide the mechanism for the following reaction (1) PhMgBr (2 equiv) (2) H3O+ workup OH
- Propose a mechanism for this reaction. || » CH3COCH=CH, H,SO4 HC=CH + CH3COH H9SO4 Acetylene Acetic acid Vinyl acetate Vinyl acetate is the monomer for the production of poly(vinyl acetate), the major use of which is as an adhesive in the construction and packaging industry, but it is also used in the paint and coatings industry.Determine the product of the following epoxide reaction in acidic conditions: CH:ОН H2SO4 (trace)Provide a detailed electron pushing mechanism describing the following conversion HCI MeOH Br2 NaOH O:
- When 2,2-dimethylcyclohexanol is treated with acid, 1,2-dimethylcyclohexene and iso- propylidenecyclopentane are the products obtained. Draw a detailed mechanism that explains this result. CH3 H3O+ CH3 CH3 CH3 OH CH3 CH3 2,2-dimethyl- cyclohexanol 1,2-dimethyl- isopropylidene- cyclopentane cyclohexene-OH H2O what is the mechanism for the reaction with the productProvide the product(s) for the following reaction: H₂N₂B
- ive the major product(s) of the following reaction. CH,OH, H* NH,When trans-2-chloro-1-cyclohexanol is treated with a base, cyclohexene oxide is the product. However, when cis-2-chloro-1-cyclohexanol is treated with a base, the product is cyclohexanone. Write the mechanism for each of the two reactions.Mechanism: Provide the mechanism for the following reactions. 1) NaOEt 2) H3O* Et,NH, H3O+