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- 2 Write the IUPAC name for each compound. Ο COC-M (a) HV Ο 0 || (d) H₂N- C (b) CH₂(CH₂),COCH, OTT HO noitos2) alodo d diw sobirbydaA to noilo ono evig of alcools dikw 39891 abitbydA (8.81 (c) CH₂(CH₂)4CNHCH, no bae totes me to slom 0 O CNH₂ با нио но но но HOOH + HOOO HO HOOOH OHO.HOOD HO || (e) CH₂CO-A iw sobixbydnA to noltoso. driw do A (D681 moitoo@) aoniMA "I w bn shomme a onions to solomeowths of elom ono bas shima Joubo aviy oj vig OH OHO bertiup bios biydisororesidenten (f) CH3CHCH₂COCH₂CH39. Plan syntheses of the following compounds. You may use the given starting material and any compound containing three or fewer carbons. (a) OH (b) Br Br- (c) ✓ -OTS (d) OH® Give the IUPAC names of the following alkyl halides: ÇI CH3 CH;CH,CHCHCH3 la) Br (bl (c) CH3 CH;CH;CHCH3 CH;CHCH;CH,CI ÇI (al BrCH,CH;CH,CH2CI If) Br CH3CCH2CH;CI CH3CHCH,CH,CH2CI ČH3
- 1. a) Give the IUPAC name of the alkyne structure F below. b) Provide the products of A through E & G: A (C6H12) Br2 B 1)Excess KOH 2) H₂O E C NaNH, D 1) (Sia)₂BH, THF 2) H₂O2, NaOH G F 03 CI(a) H3C OH (c) HBr Ether (e) CH3CH₂CHBrCH3 (f) CH3CH₂CH₂CH₂Br ? NBS hv, CCl4 Mg Ether Li Pentane (g) CH3CH₂CH₂CH₂Br + ? A? A? (CH3)2CuLi (b) CH3CH₂CH₂CH₂OH (d) H₂O CUI Ether B? B? ? OH PBr3 Ether SOCI₂ ?nane Draw the principal products of the following eactic (a) H. CH¿CH2CH, HCH,C H. Br (b) NBS hv. CC (c) (d) COOH CH,CH,OH
- Compound A produces compound E in four steps. What is compound A? A a B b C C D d E e Br 1) MeMgBr H2Cr207 1) `MgBr H2SO4 (conc.) 2) H20 2) H20 NaBr Possible starting materials OH H. HO. a) b) c) d) e)1. Give systematic (IUPAC) names for the following compounds: c)ll mobily ? 4:13 PM O 21% O < Homework - carboxylic a... CH3CHCH2CH2CHCH3 CH3CCO2H CH3 (c) .CO2H (d) CH3 CH3CCN CH3 (g) Br (h) CN BRCH2CHCH2CH2CO2H Q2: Draw structures corresponding to the following IUPAC names: (a) cis-1,2-Cyclohexanedicarboxylic acid (b) Heptanedioic acid (c) 2-Hexen-4-ynoic acid (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrile Q3: How could you convert butanoic acid into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert each of the following compounds into butanoic acid? Write each step showing all reagents. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert butanenitrile into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) Butylamine
- ST03Q3137 Give the major product(s) of the following reaction. fuming H2SO4 (1 mole) heatMelamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation fatr this reactivity.The MAJOR product of the following reaction is: (a) HO (b) CH3 OH m H3C S S S ******** CH3 CH3 CH3 CH3 + R, S H3O+ CH3 (c) (d) H3C H3C H3C CH3 R S OH OH CH3 +R +S CH3