The reaction of CH3CH=CH2 with HCl will form: 2-chloropropane 2-propanol 1-chloropropane 1-propanol Which compound has the strongest carbon sigma bond? ethylene methane acetylene ethane
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Q: IUPAC Name Bond-line Formula k. 5-ethyl-2-methylcyclohexanol I. 1,2-difluorocyclohexane
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Q: How many tertiary alkyl halides have the formula C4H9Br? A.) 1 B.) 2 C.) 3 D.) 4
A: How many tertiary alkyl halides have the formula C4H9Br?
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Q: 2-ethyl-1-butene 2,3-dimethyl-2-butene 1-hexene
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Q: 13. The structural formula of 1-bromo-2,2-dimethylpropane is CH3 a. CH3-C-CH; CH--Br CH3-CH-CH3…
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Q: Draw 7 constitutional isomers of a cycloalkane with the formula C6H12. Name each of the isomers you…
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- OChem HELP... Draw the conformational structures (chair or boat conformations) for the MAJOR product formed when 1-tert-butylcyclohexene reacts with each of the following reagents. Also, indicate if the product obtained is racemic form. a) Br2, CCl4 b) Br2, H2O c) OsO4, then aqueous NaHSO3 d) ICl e) mCPBA, then H3O+, H20 f) O3, then Me2S (conformational structure not required) g) BH3:THF, then H2O2, HO- h) D2, Pt i) Hg(OAc)2 in THF-H2O, then NaBH4, HO- j) BD3 :THF, then CH3CO2TOChem help... Provide the bond line structures of the reactants and the products formed in the following reactions and classify the product obtained as hemi-ketal, ketal, hemi-acetal, or acetal:A chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under thesame conditions, the reaction of (2S,3S)-3-bromo-2,3-diphenylpentane gives two alkenes, A (cis-trans mixture) and C.Upon catalytic hydrogenation, all three of these alkenes (A, B, and C) give 2,3-diphenylpentane. Determine the structuresof A, B, and C; give equations for their formation; and explain the stereospecificity of these reactions
- Rings + Unsaturation --- Hydrogenation If compound A C51H81BrN5O3P3 is hydrogenated to give compound B C51H101BrN5O3P3. How many rings does compound A have? Assume that P has a valency of 5. Would the answer be 4 rings? Formula -> unsat + rings = 1+C +N/2 - H/2 - X/2Rank the alkenes below from most stable to least stable.A chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2 CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under the same conditions, the reaction of (2S,3S)-3-bromo-2,3-diphenylpentane gives two alkenes, A (cis-trans mixture) and C. Upon catalytic hydrogenation, all three of these alkenes (A, B, and C) give 2,3-diphenylpentane. Determine the structures of A, B, and C; give equations for their formation; and explain the stereospecificity of these reactions.
- Which of the following alkene reactions occurs with a complete cleavage of the C=C ( breaking both pi and sigma bond components) ? Select one: A. Alkene + H2O2 with catalytic amount of OsO4 B. Reaction of an alkene with KMnO4/OH- at room temperature. C. Treating the alkene with O3 gas, followed by reduction with Zn / H2O D. Reaction of an alkene with water (H2O) in the presence of a H+ catalyst.Reaction of 2-methylpropene with CH3OH in the presence of H2SO4 catalyst yieldsmethyl tert-butyl ether, CH3OC(CH3)3, by a mechanism analogous to that of acid- catalyzed alkene hydration. Write the mechanism, using curved arrows for each step.Draw the structure of cis 1-bromo-3-methylcyclohexane and trans 1-bromo-3-methylcyclohexane (w/ all the hydrogens)
- The reaction CH3-CH=CH-CH3 CH3CH(I)CH(I)CH3 can be achieved withDraw a structural formula for the most stable carbocation with each molecular formula. Q.) C5H11+a. Draw and name all of the isomeric products obtainedfrom the monobromination of propane with Br2/light. If halogenation were a completely randomreaction and had an equal probability of occurring atany of the C—H bonds in a molecule, what percentage of each of these monobromo products would beexpected?b. Answer part (a) using 2-methylpropane as the starting material.