Question Question 1 A) The compounds below would give each of the following results if they were treated with hot concentrated potassium manganate (VII) solution. Identify which are Isomer A, Isomer B and Isomer C. butene but-2-ene 2-methylpropene i) Isomer A gives a ketone (propanone) and carbon dioxide. (2 marks) ii) Isomer B gives a carboxylic acid (propanoic acid) and carbon dioxide. (2 marks) (2 marks) iii) Isomer C gives a carboxylic acid (ethanoic acid). B) Indicate how each of the following compounds can be made from an alkene. 1) ? OH H2SO4 (2 marks) 1) BH) 2) H, OH ? OH (2 marks) HO Me ) ? + + Brz HO -Br (2 marks) iv) Br ? Br2 Br (2 marks) C) Determine whether the following reactions are likely to be Sul, Sn2, El or E2. Justify your answer(s) accordingly. NaN; 1) CH3CH2CH2CH2Br CH3CH2CH2CH2N=N=N Ether (3 marks) 11 CI CH3CH2CHCH2CH3 KOH Ethanol CH3CH2CH=CHCH3 (3 marks) CI CH3 OCCH3 CH3 CH3COCH (3 marks) NaOH Ethanol OH (3 marks) D) Deduce the structural formula of an alkene that gives the following compound when it reacts with ozone in the presence of Zn/Ht. State the IUPAC nomenclature of the alkene. (4 marks) 0=CHCH,CH,CH(CH, CH=0 (Total: 30 marks)

82NSHT The Asker · Chemistry

Transcribed Image Text: Question 1 A) The compounds below would give each of the following results if they were treated with hot concentrated potassium manganate (VII) solution. Identify which are Isomer A, Isomer B and Isomer C. butene but-2-ene 2-methylpropene i) Isomer A gives a ketone (propanone) and carbon dioxide. (2 marks) ii) Isomer B gives a carboxylic acid (propanoic acid) and carbon dioxide. (2 marks) (2 marks) iii) Isomer C gives a carboxylic acid (ethanoic acid). B) Indicate how each of the following compounds can be made from an alkene. 1) ? OH H2SO4 (2 marks) 1) BH) 2) H, OH ? OH (2 marks) HO Me ) ? + + Brz HO -Br (2 marks) iv) Br ? Br2 Br (2 marks) C) Determine whether the following reactions are likely to be Sul, Sn2, El or E2. Justify your answer(s) accordingly. NaN; 1) CH3CH2CH2CH2Br CH3CH2CH2CH2N=N=N Ether (3 marks) 11 CI CH3CH2CHCH2CH3 KOH Ethanol CH3CH2CH=CHCH3 (3 marks) CI CH3 OCCH3 CH3 CH3COCH (3 marks) NaOH Ethanol OH (3 marks) D) Deduce the structural formula of an alkene that gives the following compound when it reacts with ozone in the presence of Zn/Ht. State the IUPAC nomenclature of the alkene. (4 marks) 0=CHCH,CH,CH(CH, CH=0 (Total: 30 marks)
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Transcribed Image Text: Question 1 A) The compounds below would give each of the following results if they were treated with hot concentrated potassium manganate (VII) solution. Identify which are Isomer A, Isomer B and Isomer C. butene but-2-ene 2-methylpropene i) Isomer A gives a ketone (propanone) and carbon dioxide. (2 marks) ii) Isomer B gives a carboxylic acid (propanoic acid) and carbon dioxide. (2 marks) (2 marks) iii) Isomer C gives a carboxylic acid (ethanoic acid). B) Indicate how each of the following compounds can be made from an alkene. 1) ? OH H2SO4 (2 marks) 1) BH) 2) H, OH ? OH (2 marks) HO Me ) ? + + Brz HO -Br (2 marks) iv) Br ? Br2 Br (2 marks) C) Determine whether the following reactions are likely to be Sul, Sn2, El or E2. Justify your answer(s) accordingly. NaN; 1) CH3CH2CH2CH2Br CH3CH2CH2CH2N=N=N Ether (3 marks) 11 CI CH3CH2CHCH2CH3 KOH Ethanol CH3CH2CH=CHCH3 (3 marks) CI CH3 OCCH3 CH3 CH3COCH (3 marks) NaOH Ethanol OH (3 marks) D) Deduce the structural formula of an alkene that gives the following compound when it reacts with ozone in the presence of Zn/Ht. State the IUPAC nomenclature of the alkene. (4 marks) 0=CHCH,CH,CH(CH, CH=0 (Total: 30 marks)
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Ans-A1 if I1(KmnO_(M)OH)/(O)O+CO_(2)iii) (KmnO4^(-OH))/(Delta)2CH_(3)-C_(OH)iii) longrightarrow^(Br_(2)+H_(2)O)Ans-c) i) SN^(2) iii) SN^(')ii) epsi^(2) iv) epsi^(2)i) One Degree Halide &amp; Strong Nucledtritle will give SN^(2)R|><|h.ii) alc KO ... See the full answer