PowerPoint PresentationSlide 2Slide 3Slide 4Slide 5Slide 6Slide 7Slide 8Slide 9Slide 10Slide 11Slide 12Slide 13Slide 14Slide 15Slide 16Slide 17Slide 18Slide 19Slide 20Slide 21Slide 22Slide 23OBrprimaryStericlly hinderedSN2 or E2IOprimarySN2 or E2Strong nucleophileOClClNH22 equiv.diahlideStrong baseDouble E2BrDBUprimarySN2 or E2Stericlly hinderedBrOsecondarySN1, E!, SN2 or E2Stericlly hinderedmajorBrCH2CH3OHtertiaryNo SN2Weak baseOCH2CH3CH2CH3CHCH3CH2CH3SN1E1BrBr2 NaNH2dihalideStrong baseDouble E2Cl Cl2 KOC(CH3)3DMSOdihalideStrong baseDouble E2IOHsecondarySN1, E!, SN2 or E2Weak baseOCH2CH3OCH2CH3SN1E1ClH2OtertiarySN1, E!, SN2 or E2Weak baseOHSN1E1OOConstitutional isomersHHstereoisomersOONot isomersHCH2OHHHOH2CIdentical, achiralH BrHBrIdentical, achiralCO2HHSH2CNH2HCO2HCH2SHH2NH4 different groups, chiralCHOH3C HOHCH3HO CHOHCH3OHC OHHH3CCHOHHOABCRSeantiomersR identicalS enantiomersOOHClHR(3R)-3-methylhexaneCH2CH3CH2CH3RS(4R,5S)-4,5-diethyloctaneCH2CH3RRR(3R,5R,6R)-5-ethyl-3,6-dimethylnonaneHOH2CHOOHHHCH2OHH3CHOOHHHCH2OHH3CHOHHOHS,R AR,SenantiomersRRdiastereomersBI II II IS,S R,RenantiomersS,R diastereomersABNH2OHH2NHOH2NHOABR,SS,RenantiomersR,RdiastereomersABR,RS,R diastereomersR,SdiastereomersHHOHHOHOHHHOHHdiastereomersdiastereomersA BCDOptically active?same boiling point?An equal mixture of B and C would be?C and DC and DOptically
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