niodi~a~~d~rnaul~l~`1tli4~ai~d~flicarlr~u~n~~ ~uuBu dgn~b~aqa
Transcription
niodi~a~~d~rnaul~l~`1tli4~ai~d~flicarlr~u~n~~ ~uuBu dgn~b~aqa
J d f i % ~ d ~ ( i U n ' ~Lf l~ ~% (conjugated I fI ~ double bond) ~ I ~ $ W I UJnm~au ~ A i NI)JI~~LRAOU~~&OU~J (delocalization) 3. n i o d i ~ a ~ ~ d ~ r n a u l ~ l ~ ' 1 t l i 4 ~ a i ~ d ~ f l~uuBu i c a r l dgn~b~aqa~illu r~u~n~~ G H r ~ n a m t ~ u ~ a q d u ~ d ~ n ~ uri~:arnauua~tl~fuaudlul~n~urnirad ~duuu~u ~ d ~ a r n a ~~ria:arclouaa~~ifuaud0=:~0u1)a~tlif~au~ni~a~~a~u'1~~ u re~6~arnau *iuarddau~:~11~acnau~ o ~ t l iYf O ' U ~ U ~ U ~ ~ T~raramauuo~tlifuov~utlif ~QM uau~flu Y V Q ~ C ~ ~LL(I:U Os-orbital U V O J ~ ~ ~ ~ I Luansinu OW J uh~~darorcnauua~tlif~au~~d p-orbital / i ? ~ hrrda:: p-orbital d~1iuiir~nnrau~u~ifq d ~ a i u i r o ~ n b a u d wp o ~m ~ r fi~~iiud; ~ l i u ~ r ~ n n ~ a ~ ~ ~ ? ~ i u. u ~ u d # ~ ~ v i w a r ~ n u i d ~ ~ f i nsp2-orbital ~in ~ ~ ~ n n n . r a d ~ ~ ~ ~ u A i i ia+ u ~2 mido~ in = a ii n riusrd8aiua8un'uflunr~duq ~n~ 1 I ~ u ~ ~ ~ O J L U U ~ U L ~ ~ U ~ ~ ' ~ 7.1(n) O J U L~Lq~t (v) ~ ~ LLI ~LAW : L UL U~U~L ~ WU ~ ~ I ~ R ~ J I ~ I J i I : L T ~ L L U (resonice U~ structure) ~~~~u~utaqadijn~~~~i~~di~~~~ar~a 5 d.rmir d~sn'udd~~~d~uo~w~uii'~~"nmfau~uf~u"u ~ O ~ J U K ~ I ~ ? I ~namruuulmuuu~d~8~niw r.i(n) ~ S a r n w7.1(a) rrddhamzrflugn~au?~a~~~uu h- 7.1 (n) UALLLUU 7.1 (v) i ~ U L ~ ~ ~ V O J L ~ ~ ~ ~ ~ U u r k ~ ~ ~ t i ~ ~ u r a g ~ n u ~ s r ~ ~ a ~ ~ 7.1 u ~(tl)u d$4 ~ n ~ m r 2 i ~ n L i ~* n +Li ~ ~ W L U U ~ ~ U (resonance Y % ~ hybridj f CM,287 (H) 117 d nisnnasjn 1 naiu~iui.r~lrsni.~a=aiu lrni i d h 1 ua. a ~ l u ~ a a m n a a aMU~LLJUBUFMI~ ~ 3 MU^ 4.1 LU~I Wj~nndiaiy # ~ ~ ~ ~ ~ ~ ~ ~ Z ~ I U L ~ ~ U ~ ~ L ~ U ~ ~ ' W H ~ ~ I ~ Y riini7nmaa~hl~ul3~ufiiuna~l7~~~fiz~aniuocl I ~ L ~ ~ ~ ~ ~ J L ~ U ~ U ~ ~ ~ ~ H ~ ~ ~ V D ~ ~ A' disdao7zuiulu~aqa n ~ u m u ~ ~ ~ n n ~ a u u ~ ~ n ~ ~ ~ ~ ~ ~ u a ~ ~ ~ . i ' ~ i n ~ ~ d ~ 1) -1 o ~ u a a ~ ~ u ~ z ~ f l u d c i a ~ n i ~ ~ a ~ ~ i ~ d n a u ~ ~ I n n ~ ,a u 6 ~ f ~ ~ ~ ' d ~ I n 1 n ~ ~ f i ~ u C 4 i ~ u d u e z d w ' u z z~~a ~ ~ ~ ~ l d i 1 d f i n t w n 1 7 ~ 6 ~n71t ~si~~d~8~fi~ dfill5u1n~~~~u~z1ddu~~u~~~~fluai~~6nn'~(n'd1~1iiu~w'aun4iI~ M ~ U ~ L ~ O ~ ~ J W ~ L ~ ~ h ~ aUl hU~ Ut d~u d V ~~~J3 ~u i~nLi 7U tU~ ~ ~ lUm ~ l ~ a l ~ 1 7 ~ 0 u (hydrogenation) ( ; D J V ~ ~ W ~ 5.6 J ~ I~IRU~~DSL~~L~~U~YU%U~H'LOU~IIICIRL~~'IIIICI~U U (cyclohexadiene) ~ J ~ U ~ U ~ ~ ~ ~ U ~ ~ L U U B U ~ D ~ ~ ~ L ~ ~ C H E benzenonium ion (7.3) H& rAnrflubenzenonium ion B J ~ ~ ~ ~ ) D L ~ U X ~ ? J I ~ ) U ~ R benrcnoniuk H A U Y O J ion # k U d f i f i ? u l u a ~ R ~ L ~ ~ ~ ~ o(Lewis ~ d n ~acid) ~ 1 ~ ~d~~l(ftnfiaal[.ri1iZu83if3 3~1 dfifi3u1 / 7.a.i.e JijiiiuiLLnJit dfiR5~1B5~a~u~iZudfifi5u~~o~~aZw~u~~6n'u11.rd.rznouar~.r~uiin&uu"n.r~15j~61~~ua:~u^u'ufiao~.r6 ~~zu~+A~~~~RAP~IIH'M~~~zR a ~nlzn'u?~~uuilda ounln.rlvtflud~fi5~1diia n?flu~hu'looou(carbonium ion, R + ) d3lii~lnd~iii~l,zM-i73~afia~n~a6n'unf a 5 j 3 ilfifitmd6uwulau Charles Friedel UR: James M. Crafts 1~~7~n40dfifi5~16h dfjfit~nl(?l~1(177dfiI6~~8~63#~ (Friedel-Crafts Y D 4 alkylation) d BJ~Y"U~OUKJX RC[ + AIClp = & Al C1; + R+ (7.7) R H (7.8) 1 120 CM 227 ()I) I 7.3.1.3 dfiiiiaiiYa~dt~#~ undhu~~akt~ofln~oon1'11A nsol$~~??n#d$arvlofla~aom'l.a ng sulfuric acid) ~fa'l6qinn.r a A R ~ ~ ~ ~ ~ ~ ~ I ~ ~ ~ ~ ~ u I K U ~ O ~ ~ J ~ U ~ I ~ (7.1 1) U l ~ l L n ' U ~20 U I . 13~UHI~Rn@€lCI3 L ~ u L L I u ~ u w ~ ~ ~ ~ w H I ~ fRD ~~ ~~ I U~ C~ I~ I ~ H u ~ Y D urn1=mudasu~h~3~8~~uada~d~uflf LI 10 HUcl n 1 r a U L ~ u h L?fr f i U ~ d ~ ~ L ndiphenyl 'R 6 anhydride) halide) n n l ~ u a u l u l a f (acid lfl~h ~Jfllf Y ~ ~ ~ I V O J D Y ~ 91LflUlLIff U ~ Y O ~ ~ ~ Y a i ~ ~ ~ m a ~ ~ ~ ~ ~ a b u u ~ = :ac~liurn a ~ ~ion u afiaunif n i ~ z 7.16 a ~ acylium q ~ n ion ' ~O Y ~ I ~ c i i A ~ f l u ~ ~ h l n ~ b f l u d ~ n ' f u i u n7.17 u d 6n~~al ~nn~i a~ ~ d i j ~ f u i u n u d C ~ u ~ ~ ~ a ~ ;fit 0+- A1 c1; 0- A1 c1; 0 U RCX 122 $ AICI3 U [R-C-x I R-C-X + ] (7.15) CM 227 [H) , 7.3.2.1 r 14 va nt(n1nstbnclmu (electron releasing group) J ~Oua:aa~~ia~a/a:~~aun riasamd.r:guanlua~~uu8u rl11$miflu~icuu'laaaud~iim4u1u transition state dnaiu 3 14 u. a ~abfulnuw B ~ d ~ f i r i iactivation lri energy s ~ f id ~ On~ui~~nuddd~Unl~a~sna5~u am a tw a ~ ~ ~ 6 nan.hd~~i!tli~~nudlu~~uBu lhif M~dl~a~wna~aut!~d#o-h H~L~U~I~IUI~J'L~(activating group) Lum ~ i f l ~ ~ i ( ~ ~ ~ I ~ ~ ~ ~ d ~ (E) i j ~I ~~mi inz d~rLi i u # ~ndl~nafalf d l nd JA I J u. a u s z w ~ ~ i l u ~ ~ ~ u d u n a ~ a i f d f : n a u a : l ~ ~ u ~ n n ~ ~ y14 n kua.~as n a ~ a ~ ~ : W c # n a ~ a u ~ ~ ~ n i f u ~ u y 1 n a : a a u l ~ a ~ ~ u u ~udazaauva~nif u uaudIn~d~m0:I6~u^0~~na'~auuind fi8uniflu~duu aantl?ruuwuniw 7.2 Iaaau~uw~av III us: VIII ~ ~ i l n a i u ~ a i i u ~ u $ Ji n Ld ~~ ~~H~IGL~~~I~TIA~L~I-~ riiu~d~aaflnusrcnsil6~f an~i~ni:deii~~~ri,d~uaq &#u$dtvl~l&di~ riiu~ddaaflnus:wifi J~'IH~L#~QI~~~O=:~'IH~QI~H~L~~~~'ZIA~~ ud~mu~a~du~t#n~nf~~l~da~~~~~:~d~ aafln ~w~i:drii~~~~oaflnu'n~z~iimni~n~:nun'u (steric effect) vosn~uazaaud ~niza(3nflulua~~uu8u ~ a j d I ~ ~ ~ a n n . r a u-lR. 6 ~-OH, ~ r 1 -OR, - N H ~ , - NHR. - NR2, - NHCOCH,, -SH. -Ph (fiih - , - I 124 CM 227 (HI Ar 4 7.3.2.2 M ~ ~ R J D I ~ ~ ~ (electron A I O M withdrawing group) L~UOLIIO~M?~M~/OL(IOU (1 d~Aud.rr~u~nlu,~~uuGu ~ ~ f i ~ ~ ~ f i i ~ o ~ ~ u u ~ a o otransition u d ~ i state i m Giin,iu u~u ~a8u.riiaua: c.a m u'~diiIrr'activation&ergy ~bjuG;d O n ~ u i ~ ~ ~ u ~ ~ a ~ ~ i ~ d ~ : : n o u o r 1 5 ~ u ~ d ~ ~ l j ~ ~ ~ t ~ n n ~ o ~ n ir ~ o ~ \ u ~ ~ ~ y ~ % u ~M~II ~IJu . ~ ~ ~ n m l A dA & ^ o L ~ n n T o u o J u % o ~MI&Wn?iudod? l (deactivating group) w i ~ i d ~ ~ ~ u u l u u o ~ n i ~ d ~ r n a u ao ar;l ~ ~ u ~(GI n di n~ i ~r odd dr i omu~ LLamJ ~~ann~u l i l u u w u n i w 7.3 M ~ ~ ~ J~ aB uL~ ~~~ w I " o ~ R " n ~ 1~5 oo u ~~ i nn an ir fn a u ~ u a ~ ~ u u ~ u * u r i o r n o u v o ~ n i f u o u d a ~ l i f ~ ~ n m ~ o ~ n n n ~ o ~ ~ r ~ n ~ ~ ~.&~w"u ~~ncn~ouuind n i f l u ~ G u u l o o ~ u ~ u i uxrr ~ a u_ a .z v m a a u ~ V I $I~ i i n a i u ~ w 8 u ~ h s d q9R~ f i ~ I 6 ' 7 <; , niflu~~uulooaud~ii~~inni~~niruo~E~6nln~lv~id~ii~~v~oaflnii~n I , ( 8 n & u ~ ~ ~ m f l u ~ i u u l o o a u ~x~ ua: i u: uXI o niflu~~ualoooufhiimiinni~~nir I ~a~l~~n~n~~~d6iu~d~wif1~::ij~nwm::d~0u~n~iu~o~nir'~u~iiuu1oo XVI Lbar XVIII uamflu~iiuuloaaud~fia~inni~~ni::~o~^o~4nln~l~dd6i~~~d~~u ~ r f i r S n ~ m r d ~ ~ ~ n w a u ' ~ a ~ n i f l u ~ i i u u l a a M~IULRY o u t ~ ( ~ iXIII. u ~ ~xrv u u ~ua:: a xv uardftlu?n~mrr~iu~dfdnif ~ a u l d i t ~ a i u a : : wriilfin~nlnnirua~ . I XIV xv wuniw &y . 7.4 Tj. H E H E +- XIX Q~IUH~J ~nitn rl oonn XXII rniiuruin kH E , xxv .. XXIII XXVI drumn XXVII 7.4 &;;diquM~ml E XXVIII XXIX Id~uOor ' , " rufiur rn~m~~~aaaudu'~~n1~~81w~~u~n~=:a~n'ou Y 8 11.. ~finlutransition state dnaiu~u~u~uindyn n~uud~n.rui~~nud~ua~~~u~wdd~~or~ I - * rl w a dl~~Wnn.rouor~fin\n~.ran~n dau~~a:noudn~o~~nn~ow~::$il3iniflu~fiuu\aoau A~finIwtransition state dn~iu~aiiu~iioudyn ~~ii~~fifiiui~~nu6'Iwa~~~u~wd ww rl ornoudn~o~ann.rouo:~fin\a%inyn~ d o c d ~ u l n ~ u u ~f wn ~i~w~ou ~ a o u9ddllld i~ 1 1 1 A J E~Iina.rou d~fi5uiunudo:~fi~~uo'~.ri~fa\xi~~;ifiu a~uuod6unaiu~iui.rn'Iwni.r . l i ~ u r ' n ~ i ~ a f i u . r n i w u o ~ n i f l u ~ ~ u ~ ~ u \ ~ l~ui4ni u h ou~~~~~uu a~ fllnu l u I r a u.r.rni~ia:aoun'i~q d n ~ o ~ 1 n n . r ~ u u " u o t u " o ' ~ 1 . r i ~ f a ~ o ~ r ] ~ f i ~ ~ i ~ ~ n ~ l a w a ~ ~ u n a i u ~ ~ f l u . r r o ~ n i ~ u ~ ~ u u ~ andi?#o o o u ~6ignn~o~nnnrou iduin~n uinniiilonu~u.riioun414ilfifimdfiFi5ui~in41~l)unic~ d a i i ~ ~ o t r n o9 u#J:JHUR h~ rl u d ~ \ & ~ r i ~ d n b o ~ l n nHr~dR'dttnrn.rau ou u n e ~ ~ a i q u a t ~ ~ o u u n d ~ u u ~ Cai u u ~ n . r ~ ~ f CM 227 (H) ioun:ao~wnwdsn~naa1jm~nau~11~2 (mchlomnitrobenzene r i ~ n ~ n a u t ~44'n a? o-chtomnttrobenzene i nuiumq &u4krlu CM 227 (H) j m ~ n a I uM R ~3 2.5 0 LLnr pchloronitrobenzene C ~ ? B ~ M ~ BIMM U 8i d) 25 n i t titCuGuim3 ro an. kudrruxu I n i ~ n a a e ~sd n i ~ a d u u a i l u u Q ~ i i C a ~ ~ ~ d ~ ~ u i 1 u ~ i i 1 ~ f ~ l ~ u 1 ~ d 1 szlsiuGn 1 ~ h ~ n f \ v ( f l u d ~ i i ~ u i ~ u f ~ ~ ~ # ~ o i ' 3 ~ ~ ~lu ~~d~o~~~~ n i ~ n n ~2o ~au o ~ a n 1 n ~ \ ~ l ~ ~ = : o ~ ' 1 u ~ ~lu~b~Ruu\aoou u o ~ \ o o o u 8 ~(bromonium ~~un~~i ion. ~ r + )~ ~ ~ i i n ~ i n d j i i ? u u"u~LR=:nfno=:~8n l % ~ ~ ~ u f 6 ~ u u n i r7.23 Brz + HOAc .lli------ HBr + Br+OAc' ui~d~=:nouorl~~u~nd0=:'I5nnuouiio acetanilide p-hydrorybenroic acid rrl a R LLI (7.23) L U U ~ ~ A O ~ T L U U ~ =:lnfl; w ~mm c i i ~ a o n n n ~ o ~7 uHROR i U II ~ ~ ~ ~ i ~ u a ~ ~ i ~ ~ ~ = : n a u o = : ~ ~ ~ 4'i.s~udiinaiu~buic 0.2 ~ ~ ~ i ~ ~ u u i ~ ~ = : ~ i ~ ~ u o ~ 90% n ~ AnJ o = : ~ ~ n d ~ 7.1.2 ~ ~ u ~ u u a : l r l l 1 m a ~ u n 3 u 7.1.3 1n88u~~at styrene 7.1.4 Luu~uu~~:: styrene 1.2 O J L B ~ W ~ U ~ I ~ L ~ G L L ( I ~ ~ ~ I ~ L ~ ~ U U ~ ~ ~ ~ ~ : : ~ O 7.2.1 p-chloronitrobenzene 7.2.2 m-chloronitrobenzene 7.2.3 p-nitrophenol b a 7.2.4 p-chloroacetanilide 7.4.2 ~~I~LU$U 7.4.3 Friedel-Crafts Alkylation 7.4.4 Friedel-Crafts Acylation 7.5 ~ ~ ~ ~ ~ ~ d a ~ n z 1 m ~ ~ ~ r ' 1 ~ ~ o ~ a~c184 ~ ~ i j 6 1 n ' t ~ w " d u n f ~ n ~ m ~ t l ~ 1 6 0 1 (mononitration) 7.5.1 2 do~ifdfzno~daIdu lYfruLYuifu 7.6.2 b @ U 7.5.3 aniline 7.5.4 IulvlfL Y U ~ ~ U A 7.6 PJLG~~L~IQJHUIU + ~ i r dtnou r cofinLuu4u I?Qn~uu%u phenylacetylene nd~udadnudgjnflll~ii~~y~ LLILL~UL~~DJH~JIU - Iu~o~"M~R 84- r r n Y Brt/CCL Br2/CC14 Iuiim Iuddum ......................... ........................ ........................ A 113B r n l l l A~(NH:,); ........................ ........................ ........................ .................................................. aesluumof ........................ ........................ ........................ . . . . . . . . . . . . . . . . . . . . . . . . - niawnaed r d d 6 i ~ i ? ~ i ~ % $ ~ % @ r n ~ 0 ~ 3 1 f l ~ < ~ dua;lwa"nwnjoinni~mnwn*ndi~~da ................................................. diwlnl~rmot~ninui~~d~~m5"~~~6~1nnim(i\no~ = .................................................nS11 ~iuimuatnmm?uninleue~d~$ - ................................................... ua. -- ....................................................... Jun - ...................................................ua. - .......................................................I l J a - .................................................. ns'u Jiuimuoqnm.tinija3n~4~4~d14 Jiuimuo~nndnuu4ufh4 = ii'iuaranfu = ............................. lua u.ufumqa fidIfldfflJfi~Mfldial1~ (limiting reagent) nB ..................................................................... &4 :. Jiuim.uo~~i.rwrimn'mcy1~1na~~m5"~u~dimiuw~'1~= ................................................3ua 4 acetanilide ~uw4w maoTr~uwQu p-hydroxybenzoic acid