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- Which of the following statement/s is/are false about the reaction of 3-methylhex-3-ene with H3O+?hal. magpopost ako po then Read the IUPAC nomenclature of the following compounds and check the column where it belongs. NOTE: I need the answer immediately, once you send it I promised to give you a good rate.reactions and products for C9H8O4 C9H8O4 + O2 --> C9H8O4 + H2O --> C9H8O4 + HCl --> C9H8O4 + OH- --> C9H8O4 + Na --> C9H8O4 + F -->
- We are synthesizing an Alcohol by Hydrating an Alkene, We are using hex-1-ene and sulfuric acid. What possible products would come from this and how do I know which is the major?Write IUPAC names for the compounds below. If you use them, abbreviate ortho-, meta- & para- as o-, m- & p- (no italics).#B: Methyl acetate has methoxy, -OCH3 as the remaining of the alcohol part in the ester. Isopropyl acetate has isopropoxy, -OCH(CH3)2 as the remaining of the alcohol part in the ester. -OCH(CH3)2 is more electron donating than the methoxy, -OCH3 group due to the presence of two electron-donating -CH3 group in the former. Hence saponification reaction of Isopropyl acetate is much slower than methyl acetate. Hence the rate of saponification of methyl acetate, CH3CCO2CH3 is 50 times greater than that for isopropyl acetate.
- https://www.bartleby.com/solution-answer/chapter-83-problem-6p-organic-chemistry-9th-edition/9781305080485/when-an-unsymmetrical-alkene-such-as-propene-is-treated-with-n-bromosuc-cinimide-in-aqueous/b3feeb25-a92a-11e9-8385-02ee952b546eDraw the products formed when both cis- and trans-but-2-ene are treated with OsO4, followed by hydrolysis with NaHSO3 + H2O. Explain how these reactions illustrate that syn dihydroxylation is stereospecic.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
- Answer all questions Q1. What are the various ways by which alkenes maybe synthesized. Q2. Give two examples each of unsymmetrical alkenes and reagents. Q3. Give three examples of reactions of alkenes which tesult in anti markovnikov additionDraw the products formed when both cis- and trans-but-2-ene are treated with OsO4, followed by hydrolysis with NaHSO3 + H2O. Explain how these reactions illustrate that syn dihydroxylation is stereospecific.An unknown alcohol with a molecular formula of C7H14O was oxidized to an aldehyde with HOCl. When an acidic solution of the alcohol was distilled, two alkenes were obtained. The alkene formed in greater yield was determined to be 1-methylcyclohexene. The other alkene formed the original un-known alcohol when treated with BH3/THF followed by H2O2, HO-, and H2O. Identify the unknown alcohol.