hllia entify primary /secondary / tertiary alcohols B C Но- OH R. R, R,-C-OH Ř, 30 tertiary alcohol R,-C-OH R-C-OH H. 10 primary alcohol 20 secondary alcohol Help Improve Office Notes
Q: a. Alcohol CH3-CH=C-CH3 180°C ČH3 b. Alcohol H,SO4 CH3-CH=CH2 180°C c. Alcohol H2SO4…
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Q: Which one of these molecules is the least soluble in water? CH3-CH2-CH2-CH2-CH2 OH CH3-CH-CH3…
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A: Organic reactions are those in which organic reactant react to form organic products.
Q: H2SO4 a. Alcohol CH3-CH=C-CH3 180°C ČH3 b. Alcohol H,SO4 → CH3-CH=CH2 180°C c. Alcohol H2SO4 →…
A: The species alkene is generated through the alcohol dehydration in the sight of the sulphuric acid…
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Q: O Propauoic aad CHyCH2 COOH + H2D CH3 CH2 CO0 + Hg OT lag) [c] [c-ca] (x = degree of dissociation)…
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Q: ethanol (C2H5OH) are present in 50.0 g-sample?
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Q: H3C CH,OH H,SO, CH3 H3C- H3C- H3C- H3C- OH H3C- OH H;C- OH OH 0-CH3 H3C-O -CH3 H3C-O -CH3 H3C-O A C
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A: The given molecule is 1-butanol, CH3-CH2-CH2-CH2-OH, which has a total of 4 C atoms.
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Q: Which alcohol burned with the most yellow flame? O methanol ethanol propanol O they were the same
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Q: Identify the least soluble in water? A. PEG B. Acetone C. Glycine D. Ethyl Ether
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- Acid catalyzed hydration of alkenes except ethene that leads to the formation of which among the following alcohols? I secondary and tertiary alcoholsII Mixture of secondary and tertiary alcoholsIII Secondary or tertiary alcoholIV Primary alcoholWhich of the following compounds will be most soluble in toluene(C7H8)? A) ethylene glycol (HOCH2CH2OH) B) hexane (CH3CH2CH2CH2CH2CH3) C) acetone (CH3COCH3) D) trimethylamine (N(CH3)3) E) A and D are soluble in toluene.HURRY ASAP I WILL RATE NO NEED FOR EXPLANATION WHICH OPTIN Which of the following statement(s) about the alcohols of which their structures/IUPAC names are given below is/are true? I. CH3-CH(OH)-CH2-CH2-CH(CH3)-CH2-CH3 II. CH3-CH(OH)-CH2-CH2-CH2-CH3 III. Cyclohexanol IV. (CH3)2-C(OH)-CH2-CH2-CH3 V. CH3-CH2-OH The IUPAC name of compound I is 3-methyl-6-heptanol. Compound V is a secondary alcohol Compound III is primary alcohol. Compound IV is tertiary alcohol Compounds I and II are primary alcohols
- In which of the reactions given below is the product pyrimmer alcohol? A. I and III B. Solo II C. II and III D. I and II E. Solo IChoose the correct steps in the dehydration of secondary alcohol; then, arrange inchronological order.I - Formation of AlkeneII - Formation of AldehydeIII - Formation of Protonated alcoholIV - Undergoes E2 mechanismV-Undergoes E1 mechanismA. V-III-IB. IV-III-IIC. III-V-ID.III-IV-II Ethanol is heated with an acidified potassium manganate (VII) solution. What would be theproduct of this reaction?A. EthanalB. EtheneC. Ethanoic acidD. Ethane ALL of the following Ether can be prepared by Williamson's method, EXCEPT:A. Ditertbutyl etherB. Ethyl-tert-butyl etherC. anisoleD. Both A & B. Which of the following is not true of SN1 reactions?A. They are favored by nonpolar solvents.B. The concentration of nucleophiles does not affect the rate of reaction.C. Tertiary alkyl halides generally react through this mechanism.D. They occur through a 2-step concerted reaction. Butan-1-ol is formed from which of the following reactant-reaction pairs?A. Butanal - reduction reactionB. Butanone -…#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.
- What products would you expect to obtain from the oxidation of thefollowing alcohols with CrO3? a. Cyclohexanol b. 1-hexanolAlcohols A and B formed layers with Lucas reagent within 10 minutes. However, compound A formed brown precipitate with KMnO4 while compound B did not. Which are the possible identities of compounds A and B? a. isopropanol and tert-butanol b. ethanol and methanol c. propanol and tert-butanol d. isopentyl alcohol and isopropanolAbsolute ethanol (100% ethanol, with no water) cannot be obtained through simple fractionaldistillation because of the lower boiling azeotrope that forms with water. Propose a method by which onemight prepare absolute ethanol
- IV. In every chemical reaction, include the IUPAC name and draw the structure of ALL organiccompounds present.A. Give the reacton on how to convert the following organic compounds. 1. N-Phenylpropionamide to alcohol 2. N-ethylbutylamide to alcohol1. (a) Which compound would have the highest boiling point? benzophenone toluene acetophenone benzaldehyde (b) Which of the reagents listed below can convert a primary alcohol to an aldehyde? H2CrO4 DMSO, (COCl)2, Et3N AgNO3 KMnO4-, NaOH (c) Oxidation of alcohols involving the use of DMSO and (COCl)2 is also known as which of the following? Jones Tollens Baeyer-Villiger SwernNaphthalene, C10H8 is insoluble in water but sublimes easily when heated. How could you separate a mixture of naphthalene and NaCl? Suggest two different methods. asap