Which is a synthesis of 3-bromohexane? 1 eq. Br2 H2. Lindlar NaNH2 1 ед. HBr H2, Pd/C NaNH2 1 eq. HBr H2, Pd/C NaNH2 1 eq. Br2 H2, Pd/C NaNH2 1 eq. HBr H2, Lindlar NaNH2
Q: 9. Which SN1 reaction in each pair is faster? a) b) (CH3)3CCI + H2O → H,O (CH3)3CB +H0→ .CI H,O
A: SN1 is a unimolecular Nucleophilic substitution reaction. The reaction involves a carbocation…
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A: The given reaction is a type of nucleophilic substitution reaction.
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A: The details solution for this is provided below in attach image.
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A: Introduction: When a carboxylic acid reacts with alcohol, its forma an ester product along with…
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A: Detail mechanistic pathway is given below to find out the final product
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Q: Which compound is the major product of the reaction sequence shown? (1) NANH,NH3, -35°C (2) CH3 CH2-…
A: 1) first reaction is acid base reaction. 2) second reaction is SN2 reaction 3) third reaction is…
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A: Given:
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Q: (1) (2) (3) Reagents a Br2 CH212 / Zn(Cu) / ether e i 1. O3 2. Zn / H30* b. CH31 H2 / Lindlar…
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Q: C. CH;OH Is this reaction E1 or E2? elimination product(s) d. NaOH Is this reaction SN1 or SN2?…
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Q: CN CH2CH3 NACN PQ-6. What is the rate determining step of this reaction? Hirgh H3C OTs acetone H3C…
A: • For SN2 reaction Nucleophile attack from Back side .• In case of SN2…
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Q: Which halide is most reactive in SN2 reactions? Select one: CH2CH2CI ÇI CI H3C CI CI CH3
A: The reactivity order of SN2 : 1° > 2° > 3° alkyl halides.
Q: Part 2: Simple Reactions Draw the structure resulting from the following HC1 + HOCH₂CH₂OH CH₂OH Dess…
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A: Hello. Since the question consists of multiple sub-parts, the first sub-part shall be only solved.…
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A:
Q: 1. What will be the major product for the following reaction according to the Markovnikov's rule?…
A: Note : As per our guidelines ,we are supposed to answer first question , Please resubmit the other…
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A: Soln
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A:
Q: NaOH -ċ-Br 50°C
A: See answer below
Q: Qs1 Propose a correct synthetic route. Can be more than one. ÇOOH NO2
A: Since you have posted multiple questions in a single session, we are entitled to answer first…
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A: This question is based on the Electrophilic aromatic substitution reaction.
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Q: OsO4 and NMO B. Br2 and H20 C. Hg(OAc)2, H2O and NaBH4, NaOH D. RCO3H E. BH3-THF and H2O2, NaOH…
A: Ans) BH3 and H2O2, NaOH
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Q: Draw the substitution and elimination products.
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A: Applying concept of organic synthesis.
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A: The SN2 reaction can be best carried out with --
Q: II. Multistep Synthesis. Supply the missing compounds/reagents. H,C BH, EtO HBr FeBr HC H,C но. Br.…
A: We have to answer the given synthesis.
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A:
Q: What is Lucas reagent composed of? Choices: HCl, ZnCl2 CrO3, H2SO4 Sodium nitrite Iodine None of…
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Q: 1. 1eq. Eto /E£OH OEt 2. H30® Dieckman cyclization product ОН Anhydride NH2 1ед. 1eq NaOH O=
A: the detailed mechanism the structure of reactant or product will show below in attach image.
Q: CI Br. NO2
A: Answer:- This question is answered by using the simple concept of chemical reactions of benzene…
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Q: 56. Rate of SN2 reaction: I. CH;CH2CH2CH2CH2BR + CH30/H2O→ II. CH;CH2CH2CH2CH2BR + CH3O°/DMSO→
A: We know that SN2 reaction is second order reaction because it involves the nucleophile and the…
Q: Provide the major product in each box for the multistep synthesis below. Mg0 1. H2SO4 Br Et20 2. aq…
A: The reactions given is,
Q: What reagents are needed to carry out the conversion shown? HO HO 1 mole / H2SO4 2 moles /H30* O…
A: The reaction taking place is given as,
Q: What reagents would you use to prepare product A with good yield? ? CH3C=CH A O a 1) CH3CH2CH2CH2l:…
A: In the given transformation, first of all, an alkyne is deprotonated and then alkylated after this…
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- Which base would be best for promoting elimination over substitution? a. H20 b. CH3O- c.(CH3)3CO- d. CN-Choose the appropriate reagent for the following reaction. A) TsCl/pyridine B) SOCl2/pyridine C) ZnCl2 D) PBr3 E) HIWhen toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2) groups are substituted for hydrogens at the 2, 4 and 6 positions on the ring (the next section discusses why the 2, 4, and 6 positions are substituted). The product is a highly explosive substance called 2,4,6-trinitrotoluene. This subastance is commonly known by a three letter name. What is it?
- Use E1, sn1 or E2, sn2 Synthesis1. What type of reaction is occuring in step 3? (halogenation, hydrohalogenation, reduction, keto–enol tautomerism, dehydrohalogenation, acid-catalyzed hydration, base-catalyzed hydration) 2. Which reagent is necessary for step 3? (Br2, HBr, H2/Pt, NaNH2, H20/H2SO4/HgSO4)select the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO4
- Draw the organic product(s) formed when CH3CH2CH2OH is treated with each reagent. a.H2SO4 b.NaH c.HCl + ZnCl2 d.HBr e.SOCl2, pyridine f.PBr3 g.TsCl, pyridine h. [1] NaH; [2] CH3CH2Br [1] i.TsCl, pyridine; [2] NaSH j.POCl3, pyridineSupply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2Complete the following reaction equations :(i) C6H5Cl + CH3COCl →(ii) C2H5NH2 + C6H5SO2Cl →(iii) C2H5NH2 + HNO2 →
- Draw the major organic product of the SN1SN1 reaction:Minor product via E1 for 2-butanol and HCl?Rank the following species in order of decreasing nucleophilicity in aqueous solution CH3COO-, HO-, CH3OH, CH3S- Select one: a. CH3S- > HO- > CH3COO- > CH3OH b. CH3S- > CH3COO- > CH3OH > HO- c. HO- > CH3COO- > CH3OH > CH3S- d. CH3COO- > CH3OH > CH3S- > HO- e. CH3OH > CH3S- > HO- > CH3COO-