12.C6H5COCl13.14.CH31.CH2N2(过量)2.AgOH??15.CHO+OCH3CH3CH3CHCH2NCH2CH3OHCH3COCH3OH /HO2CHOOOCH3CO2KCH3COCCH3?3Al[OCH(CH3)2]HOCH(CH3)2??CO2CH2C6H5H2/Pd16.O三,简要回答问题(8分)
1.蓖麻酸有几种旋光异构体?
?
OHCH3(CH2)5CHCH2CH=CH(CH2)7CO2H(蓖麻酸)
2.顺-1-异丙基-4-氯环己烷和它的反式异构体分别用NaOH/C2H5OH处理时,那
个反应速度快?
3.下列化合物中哪个具有手性?
CO2HHBrHBrCO2HACH3CH3HC=C=CC6H5CH2CH2CH2CH2CO2HC
B
4.下列化合物中哪个不具有芳香性?
CH3CH2CH2N(CH3)2AB
四,封酮(Fenchone)为一萜类化合物,可从茴香油中分离得到。外消旋封酮可由以下路
线合成。写出合成中省略的中间体及试剂(a)-(n)的结构。(7分)
CH2=CHCH=CH2+NHC(a)CO2CH31.(b)2.(c)CO2CH3CO2CH3CO2CH3CO2CH3(d)(e)+(f)1.(g)2.(h)HCO2HO(k)(l)(i)CO2CH31.(j)2.H3OOCO2CH31.(m)2.(n)CH2CO2CH33.HCH2CO2CH3HOO2NaNH2+2CH3IO(Fenchone)
五,写出下列反应的历程(8分)
H3CR1.OCH3RH+2.
六,用简单化学方法分别鉴别下列两组化合物(8分)
OHOHOHCHOCHCH31.OHOCCH3NaOC2H5OOCC6H5HOC2H5OHROCCH2CC6H5OO
OO2.NHO
七,完成下列转化(12分)
1.OHCHONH2NHCH3
CHOHOCH2CH3CH3H5C6C=CC2H5H2. 3.C2H5HCH3CCOHH5C6BrH5C2O2CCHCO2C2H5NH2(CH3)2CHCH2CHCO2H
八,按要求排列顺序(9分) 1.按亲核性强弱:
CNCNNCCNCHNCCNCNA
2. 按酸性强弱:
CO2HOHCH2CNCCO2H
BCO2HOHCO2HOHCH3 A B C D 3.按碱性强弱:
CH3(CH2)4NH2NHONH
A B C
4.按SN2取代活性大小:
CH2CH2CH2Cl
CH3CHClCH3CHCl
A B C九,化合物A,C9H12O,它的IR和NMR数据如下,写出A的结构。(6分) IR: 3450cm-1(宽峰),710cm-1,780cm-1
NMR: δ0.9ppm(t,2H),1.6ppm(q,3H),2.7ppm(s,2H), 4.4ppm(t,1H),7.3ppm(s,4H)
十,一个药物Bromodiphenhydramine(结构如下)。它的合成原料之一是 2-(N,N-二甲氨基)乙醇[HOCH2CH2N(CH3)2]。①由适当原料制备 HOCH2CH2N(CH3)2。②以2-(N,N-二甲氨基)乙醇,苯和甲苯及其它必 要试剂合成Bromodiphenhydramine。(6分)
BrCHOCH2CH2N(CH3)2(Bromodiphenhydramine)
十一,由丙二酸酯,甲苯和不超过三个碳的原料及必要试剂合成:(12分)
CNCH21.CH3CCH2CHCH2CO2C2H52.
CH3CH3Br
南开大学
1993年研究生入学考试试题
有机化学
一,完成下列反应式:(31分)
1.BH32.H2O2/OHCH31.(构型式)2.4.HC=CCH3CH3Cl2/H2OHHCl(构型式)3.CH3CCNa+5.CH3CHCH3OHHCl6.OCH2CH=CHCH3CH3OHOOCH2OHCH3CO2HOH8.7.CH3CCH2CH2CH2CCH2CH3HOhvPhNH2CHCH339.10.HHOCH3OCH3CO2HLiAlH4(构型式)11.O12.HO2CCO2HCH3CH2OCH3OOHCHCOCH3314.OH13.HCl(干)HOBrOHCH3BrNaNH2Br215.16.SNOCH3NOH17.+O18.CH2CH3OOHH+Br2C=C(构型式)19.HO2CCO2HCONH2OH /Br220.CH3(构型式)OHHCHCH3H?OCH2OHCCH3OH21.CHCH3CO2H?CO2H
22.23.24.OC6H5CH=CHCCH=CHC6H5OOC2H5HCl/H2OOHOH+CH2(CO2C2H5)2NaOC2H5 +CH2I2NaOH
25.OPhCO3H
二,命名或写结构(5分)
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