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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)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) Butylamine1. Give systematic (IUPAC) names for the following compounds: c)
- 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.3) How would you prepare following compounds you may use any other reagants. LIAH, но ??? MeMgBr