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The document discusses hydrocarbons, specifically alkanes and alkenes, detailing their structures, properties, and methods of preparation. It covers various reactions such as hydrogenation, dehydrogenation, and halogenation, as well as the combustion of alkanes. Additionally, it touches on the stability of different conformations and the chemical properties of these compounds.

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0% found this document useful (0 votes)
6 views

hydro (1)

The document discusses hydrocarbons, specifically alkanes and alkenes, detailing their structures, properties, and methods of preparation. It covers various reactions such as hydrogenation, dehydrogenation, and halogenation, as well as the combustion of alkanes. Additionally, it touches on the stability of different conformations and the chemical properties of these compounds.

Uploaded by

atharvojha005
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
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“WAC Compounds Contant only carbon and hydrogen ON Calid pyeluocanbon Hydiocasbow - \ . Opanchatn Closed chasn Satudtid Unsaturaud \ Altane Avene Altyne x Benene A\yanes / Por of fe © Hyduocabon contains Carbon Carbon Singt bond » ° Thus genial yor uta De gue of Carbon s — ace hat | ae | ii Al iphatec Avomaks c 4 CuHansa CHa ion of Alkanes Ds => meshods of Prepuation of gabaleiy- Senclerence Kes © 8y nydrogcnation ef uncatuvated hydrocatbow . Adkevas / Alleys suduced in precenu ef PL] Pd/ Ni $0 yy qe alka Ren at Py3 KC: Yoom demp - CH) =CH, + Ho a CHa— CH3 ethene ethane . ethy Low Ni/oaak CH3~CH=CH —CHy t+ He —*— = CHa-CHaChicly But -j-ene- Butane (2) Wusdr Reaction — Two simitar moliut ol, Aitye abide suact with sodium metal im the poucience S Diy ethun to form abkcurs yuth ewe ne of casthon : "| Dey be ye t ne CHa- Cla 4 aha ae ethane Go tana — > : 3.3 Dimerhyts butane Ha CH -CH3 a Ha Dry ern cha OMs aad bs 4 Na, Can ; cll ca Cry yy wrun +0 dup, alkyl hatids Involuus tn we 2 veaction to form Mixture of ther alkane she th ast df puree +0 separate © BNa/Dry Srhu CHa + tHe —H BF eg CHF CHa CH, -044 4 CH a-CHa-CH a -CH Chom yorty came B-p- cam"+ be ceparated ) : ake CHa fatebs city Cla BA 4 ana Sg cy cery thas ~ cua Butane - 4+ anabe ernyt Bromide. CHa CH TCHS CHa Hy ; ~ erg OH HC CH TIM, diard- 3-Tetramithyf puran® { ' i 4 4 ae Me —— tile ew esepepecgpepuguETOeCOuevvvv™s ™SS @ Reduction ef Alley! hatrde = UHa-ce pHa NES oy te Ni CHa- By CHA Ni + Ho —— C ‘J + HR | Cuabor yll ¢ OD) Decarboxylation — when Na Or bk salt © ans 10 que au yeadd usiih soda tome (Noon 1 CaO) attans usitth J carbon UNS ° 1 cia -f- 8" cace rete ) Oo baat Y te nla” ce odivum pclae) - example IT oe caO- ( GHla- Cooma 4 Nao ———> C4 4+ Narc04 + ou 4 ROOM Cy y “CHa “CHa, @ CHa -CH2 OP = cooNa “eyo 4 Naic0a LgoNa Be: ~ cad E Oo 4 meet (c) + Nal03 es electrolytic muthod col of Ma/k Galt of kolo Elect vous! s of a quiew couborylic add 40 form atan at and ds Electyolysis of godttun autate 4aNa' 2 CH y-COONa —> actly — C007 H20 —> HH! 40H” At anodi > CHa - fae necs qicoo —s> CHa- cH - ial oe 3 2 t Fast de At catnods ant dae —> Hs t exly AO Ww : o Khow Vedyo ve (Hs $03) mole valuncy C1) Sub phuxour ac Kuss valency (ous) salt * = > sath > the 4,60, (Porta cutphite) fe > salt > ale’ Sulphuric oud (Ha804) ay toe wNo, 4 MaNo, (Nusite) uh Sie panos cptitral) yosoa (peta: dove hy wth HT o 6) Avi hatids yeachio — CH, FHBYAT> pe | aHT —> Ora — | HL > strong QA” ‘\ WNYA > siioKg O-A Crta-Cra- on of abtohal ,aldthyds » cambory iit acd’ @ peduct! (67 07 . > Aicohas fs Matyas AOF s carboxylic — aud Aleane — cha ced crs 4 Qe — > coats 420) +e HW : ay Ped P- ©. thy cH = 0 4 AAT > crlancrla tHaO fF OTa ft @ {es ped DP \ CHa-CroH 4 6 D-CA Hach 220 t 2E, @ CHa- cH OH ‘ 6 Grentouae- tn wus owuy unt Red P 4 Ren Paw’ Seale Rare) P oe ‘BEynunbucds odd nov oh caxkon ’ . R2WUet +R UPR) 4 4g RUE wT > Ratuli Ce as EEA SSS SSE ET EOC Aa Free vadical! ushth veack utith nid val al (1) Alkonss coulsolubl in wali bcor ty ot pol poet 4 RS @ CU ae rice oa ee CHa Co- tn > liquid Hor 4 crac ma on mg y | Claetea —> sold dix waal ui duu +0 urtak vor (> Ber of atkane is lo ap a sive) forces = @ BP hes sith Muu ase © As (mouasc Oo: Of Branching BP L Cvandu wa im mo of casthor - é > a eee > c-tHe ' \ c(iso ) C tueo). ef casbon 1s of cartben- c-¢ oP c-c- 6 cm. Pentame) meP of alkan haung curr ne waar than alkanm hauing odd wo but (00d ont shoutd be neigh bor ) - ls L6e 2Ca KRCa Fla Lei0 6 mer pes CHEMICAL PROPEPTIES OF ALIANES (Vy Halogtnatt on _ eAlkanes warty show free radical SUbSIHUON ¥xn - Qa Chloriwadcon hv 4 t fe ———— > CHa-oO +Ha- Ha Mec ‘ \ echauu mM > thu rin dake place im 3steps ounce prods Hee radical» mods —————— te Nawitiation Ut g Bee 6 4 1) Chain Propagation: ly 40 = Cts HH CHy + Ur > Ha 10° @ Haintermimalion cy, p cry > CHa~ CHa CRY prectuct ) (®) Bio mimaiton CWHa- CHa + Bis > Chla- CHa BY + HB - ee > CHa-cH (Hg- CHy + By > CHa — CHa -CH3 “) \ \ Nee un CHa oa 2 + HOy Areautividy 2 329821" CHydiogen) > Hatogcn subst duce 27> Po IL Hydrogur) ua 2” : Bra © Jodtnaoh Gh 1s leuucible Pou bceor formed HT (siren fhat's y lodination dakes plau in pwesence of (strong OA HMOag/ HIOg ) HNOg (Ha 4 o> _ Ea Crla—er 4 HT: ay q PA) (A) Jamon ination Direct {Luorivatton werplosive so atky) ja oridt fOrwud induudly © CAGE / Hae fe ; CHa 4 Bx2 7 CH3—Bs 4+ HB CH4-Be 1 AGF —> CHaf + AgRa’ \. Readividy ¥ b . Fal Ba,7h? 17 a OE 2+ dxidabion of Alvanes — (a) (ombustton — Alans on combustion gus la ge omibunt 6b brat that's why ty wed as fuel moa * (ntl) #20 | CoWanada 4 (Bett )o— \ x ) ) (ray + +o, —7 20037 ZH20- > 3 > CAH + L202 > 400 4S HO > 2 Py) Imcompulr Combustion + ; shin alran Inco nepltely oxi dire bo que castbon 5 black ushech is wed ty naking of ‘ink - e (4 408 — ¢ +4 aHs0 . (Corbon Black) (ny(00) 3 © Calolytic Oxidation © o 3cH2 CH3 | 30? ——Zunyroow . Gu / 593K tahD oe nae 0s Team > HATO Cmuthanol) 2 Mos 03 ‘ CH4 +08 CG (met hanal ) . ek Kmnos cha ‘ 3 CHa-t—-H SF (Wyg- 6 OH. . Y ' \ , ee ie cha (@) _Teomucrradion , Altay walty chow cham iso win Mm - uv \ -— Anhy: AV i (Ha 7 CHa CHa fay cai CH 4 NN dis Bowuty! (4) Avomaty ration ~ When alkans h a yn aus 6 Cosh a ys neoktd af 443 kK in the pounce Of “ : 1104 Mor 0z 40 qiur dehydyogenation ren am be vy “m Nvomatiialion > formation of hensene CobHyg ( Hexaue) py TSX y cH Gy C4504 cH “i b1 44H t \ > Sl \ > CHa CMe TIAK W a me ei ¢ ‘ 7 NZ ' . CW lepiane . N20" > Heprane - eared —— ToLunic za 2? JIS k lO dt Shoutd" be Heplane - © Pyrolysis /Caeving & Wights otkauu lucid at hgh : empuratue fo form smatix alkane or alkene the ss catted py votysis - Used to Com Kerocene to cil qouoy prbrotiim High alkane — 4 Aiea d nike: iqh CgHig Mah aeme Ca Hg 4 OHe Catton) CA\Coue) . Conformational (soutien. ° amp —- THE fsonerum shown by euly alkauu dut 49 yotarion ©} Carbon astound © Single bon d - 4 (D Ethane = @He = ee ! \ caus worees 7 Nth on A 1 "ih NZ" \4u i eitipsed we \, a agquud - ‘ ' 4 4 ‘ ‘ e e e 1 = ditedwal angts = 60 Newman ine = NN ‘Oy ection Nt ew Teicional taunt Sha oa Wor ctabas. ein ae Skew “IN Cli peed form forcional ctrau (Repulsion force ) } Vs maxincum thal's uhy It Te heast StodSe- ° \n Siagqucd form torsional strain is O soit has moxinim stability - ) : ) ) > : Sdability ordurt Stagquud > Stee > Euipsed - o *bnergy diff b/w eclipsed and Stagquud te (af bY note! . . * . , P&Uipsed hauc more enugy than Sag gured - bxampte> Busans - CHy— CHa CHa CHa. CC4Hi0) y cH cH aH thy 4 ’ \/ 4 , , 4 , H uO ; CHy 4 sta ed (more <+abir) on scp : Staggered ( dw . ki j oon ow Ww. OH " i wack 3 tig Ope NO He ona nfo on : ‘ ont Ae tvce PRepudsion 4 4 ee con ut) sy Alkenes \( Double Miedad tiyds ecarben ) Geneva forppula > Cutan. Methods ef, Prepeer cd ion Se ee Ue oa eb (1) Recuction (peutial ) ef \W psscnce ef Pd=c (Limdton Calatyst ) Ssometimus Pb Basog + Pa Jc WWE CH + Ha CHa = Ga Einylene dv Eshene Audylene oy 6thy ne - I Denycio halogurat! on—ef-Alleyt watidle & — \n—pouscncoef ake bor 4 4 gyn add mp. oe y= J (ws) “= sy Nona CHa CEC CH More at Wa/tiqg NH3 FH Cry Oh Wy droge But - a yne a Soca Ceram) a, Ny ant add 3 yw ove paid aks CHa CH= (Ha Propyne domot show te Te acs haynrla Lia Ca - CHE Cha ane (a) Dehydrohatogenation of atky) wis a , Ion prreuce of altohalic Kor Alky! hatids edad akiBholie KOH ho form athent . dus wa &f eLinscineatton readion : —_— OOO ce omne \R - elimination of H) © CM S- eH au asio a ta ° 2 7 & 1 oH tt et KUT OD & Saytret, prouicds ability of ateene: cw CHa voyoa Pp ron eo (Ha- CH —CH—CHs > (Ha-—ce=tH - Cha B | ale q 2 3 ii By » ly Se kou | 4 7 cH ——> crt, =Uha + kU 4H20 Il alco woo& 9 eaportambk “© Says re} 4 Rule > ; \ ela . > * Durcng eUmmation rin hydvegin Cue ‘ _ " - tece mo. ek Hydregin > F Corbon ushich conturus | > = XN Boa e my” CMa CH CH Hg 4 von E> cua ce CH CHa , 1 ra + kCR + HO = = = = = = + KBy + Had d-Mesnyt bul - d-ene€ . . ovdin ef dehydsehaloquualron o Tp Br? Bs atky) > aalky) > IPatkyl- @ Vehatogeats on of -dthatd din aticlu. + — - cH . . danatide ee ides duno de * u (Hy ow gueinas duo t - ~ Oo SHEITIIVIIII SES aS ‘Midimal dthatide rea Ucith(2y Metal) yo joryn athens —_> cn 5 9 i yo 42n ———S CH= (Wa 1 Pra & u Ethyrenc @ Dehydration of Alconal ‘(esasptoeth) olm presence ok concentyatsd Hobo, Or Ha PO, ' Ov ALOR /623 40 gue alkene © re ths- dis-on CONE. H5604 ' - a EOF Hi Ethanol or ety! alco e F eo & (Ha- CH - CHA Cone H2S04 \ .s Tom CHa CHS Ona Prepan 3}

1° at coho!y ‘ ‘ Sy PhysicatPropuctias Of Mkencs 6 - ® Mkertx wu more veattive phen alkanes dus 10 frercare AN bowd . bond we uLeaker juan o- bond that is why V4 behav eich untye a Boiting point of atkens Ts greats tham atkernes ALU r so to Polasiity - , ° \Soliibts Tm wader . X F : ° : : Altes marily show geometrical “Teo mcm (Gs/4rave) , Chae ‘Isonarismand position Isomusim ) pohemica pro utiu: ee bond is e~ vith) > Alken Matily show Clatrephitlic Addition Raw . din fodouble bond « — —COS: / (> Room sew p- (1) Reductiens % In presence of Ni, PA, Td ta 4 H-@ ——> Uta- ata & a ey hy tense er nyc chfovtcle — Add of Halogen atid Vo wnsynrntetses cal Mayr ni kov Ruto eureies atkene , neqatiue part added Jo Carrbort which dw No Of hydrogen : Gb 4 WiBy——> cua CH Oy fHa— CH= Mechawusm “= o . . . 3 5 5 y y 5 ’ y y 5 y , ' Meni avium _ (Electrophilic add™ H- Br —= pty Bs + AH x CHa- CHEECH, OWT oy 1 Ba" —> (Ha- CH CHa — J oe 2° conbocaton more stable E xewuplt | cH _ : - CH CH= e aH WE CH 4 wey SR aac na An = By a ape o™ , e CHa- cH CHE tut = ea c HTN \ cHs CHa Hydride Shupt BY Hyon \ + (Hg ea NS eB cH CE CHa CH | ae cia, 2° Cuntocation move crable Gana. oe @ CHa pH Ne — > ny —b— ta — thy : cas TTS . CHa ) 7 . ‘ cna \ Metty) Shote ) | Wows CHa 6 a Hg ; \ ate @ & . , A hy dude chift / wetvayl sy J pry) «leh ue pen — CH ONS x Avcit mot Fi Wi kov Rude s Guy HRs addid FO Gay | atkens in thx psurscnce Of Ov game puro dt Lognsrls Benroy! PUoxide | mi gains park addsd 40 carbon usbicl comlaimk maximum no. of Maydstoqun Aw : Avi imou Mechateet © (tree vaducal { al reaction) ‘ ' CH= CH = (Hyg tte ereieee , : x ) m (Ha-Ha WP “ Bromo propane 8 HB of B a C a By > ° Pa Panov ide Ci, Cant imor tinikow Pal ) \ (@_ Addition ef Hatogur =! Mostly ( Uo, B33) 7 qorm vednat duhaudt ) cmoreinikey wwweg uuu vvree Ua, Bas tread with alkene 40 Aquous Bra so” CReddisn Brown ) nun Corot pecomne Colours vshen reacl wits athens OF abkyne > This b at of unsactuatier a CHoaCH2 + Bra ays cH i ; a>— CH? ’ / cole 1 1 Br BY , aco Y cach =crls 4 &s —> cHa cw — cH ‘i nr \ \ ic aw / : . : . as + ® Diytic areminatson / Ciprinodton > fafa 7) puy lie €or ben” = bond o> NBS CO Norma Bron (m- Brome Suuina 4.) nev to = es | ° a ot” Brom. suucinanidt ) penrytie coxben | 5 gh is vespowsible {or any ¢/ snert ke benzene 2 1 one Benay lic prow nal lor () co NBS do nod yead al, double bound - o cH He CHa NBS cy — CHE Fe ae \ \ NN 2 ey ky Br eo A 0 A ow - CO > C J‘ ey 4 . en wes Nuits Cy Allie or Bemaytic Watoqenatton also saves plare al hugh fem purccture 4 Bas 7 Ua CHa ae Cra 88? ~ CH CHE CHa aaa \ \ a) Naluat qos OWA) Cote 1 Ko HRs Leas [> Wa- OH CH Cation Cae By PA eon HB -CH= —> = 3 > Peroriy; CHa Cla. Cha~ Bx J NBS Wa ene CHa Bey Be (cascaees CHa cw a UM \ aq: Baa a can (Ha —-t4 —cHs a4 ! \ Ba RY > Watt i a wou wok elrcbtoluce * rveact with dtkene jo form alocokat acoyding +o Mastkinikov wttth a reasvecing Uren + CH, = Clr 44,0)" = Uta CHa-oN- CNuylew Nt one 3 uw . 7 (vs opropyi adcohal) CHa-CH=CHa + Hao) 4! chy dH Un 1 +9 OW +0 form atleohal - ooh as Shim plx addition of w otut opposite oF mosnikov suule - CH. CHa acha-cW = CHa + eds ——> ove oe oe d . cng one Oe 6" ay Bake os "owe i cH3a- CH =CH2 ~ > CHalH, Go 1 v Racauaas 2H20H Ht Se } - - _ “ . a a , : ry @ > CHa Ch CHa CHy jrLA CHa CHa oH: Hycbucle shuge (hat - a) one * @ SU ot tee CHa - 0 CH CH? CHa (Hs BO Hate Alkene veact Witt Borne Bro B diborame Bats foitoused by HaP> | Crla- CHaOrk +B COM D3 ay] W202 > 20H 3 Ha a HgRO3 | To avoid yearn gunent py uy potion iM mastkonikoy vule thy Woo wn -) add* ef H20 WLULLLLELOLL OM —— WUsy wird cal _Oxin uusyrcdion = De We | sim c autoke Coracoo}e ta or Sting te fosround bY NaBH4 to {o1m alchul ° h according +0 masekihikoy wWitheu suave Z (r@rateo at CHa- CHO CH = CHa eeeunee wach § Ho Wa ov fe a (Add Uo) Summ Wye = Makin bow ws bre “ ow GH, HoospHt da tie Ce ee ~ee CHa Cia Cus 5 ns BaH os Anvivmwuinikov—> LB2M/ 202 oy tO eae CHO CHa ' noe i Os : mon \nthoy LNA)? J H20 gk — CH tg ; wWathout pean tugewrt ' eMrIN a BY g cus On ; ‘ 8° Orowolysics ‘ —_s ‘ 1) Compound comacning doubles tips: bond 7 read urith oO20ne (03) +o que ponide:: : which ov Frydvolycic que atdinyde CY Yetohe : “oo pea. ae N ; 1 ‘ : . 4 ps CHa CHa 403 —_s 4) ch, -2eP2S CHO ; rye | +Znd + ! ( | oO oO / Lao 1 ozowde Hg -cHeCcH o 7 © CHa -cH 2403 SN Rr CHa- ce ch 2 ———_ > =n.0 \ 7 Q CHa-CHOTH CH | / o-f ‘ Contalas hyde) ' 2 CH3-C=CH-CHR )- 3 i sm tH3-¢ cH (Hy For reyisen a - a — CHA ; 20/20 ' ‘ Cie 4 CHa- CHO o,° 1) 03 CHa ; ‘ cad He CH3 se > 9 CHa CHO 4 ' '') 2p ftir ' \ o - | Q) CHO su can gl e6- died maa co & “ee Wo 6 : 0 Chan, ( ‘\ ~_1) 03 cue 4 CHO : e Pd | Jono : Vy ows ta ~ e\hy len Rulan- 14 dios yuyoxal Quy aS AY atten on Orornu dyes que pro panone A me wmethanal usutite tle formula of atkene propa > cWa- t=O \ ows CHa Meth uadl > CHa.2 0 NW cua —¢ : \ CHa (Wa 6S O + OA CHD => (Ha -c = CHa ch oy 7 ee @) Oxidatiov_ of Alrene _ @) Bayt's Reaquit = — Cold, ctucts atkatt sol” © of KM nay | 4s cabudl Bayur's teaguual * (i201 0) CHa = Cha + RO +o _Alkottue Cys — Chto KM~n04 ) > ) > = _~ = 2 = = 2 = ~~ = : 2 1 | 2 lat ow ol . ou erny tune guy col 1b) oxiddtron usith cu dic KMn 04 . ———__-—— . = ly 0 HO = (UW ~ CHR —=> Oh- (00 H. Catid ) 2c C—Cn3 — Gimme o= 4, —-) Caetow } I, om on 4: kMn04 Gig cut cls + (04 > Ha Coo 4 (024120 cea H c ! a rt CMa ¢ = cH-cH 3 {04 = oe ca eas ft CH3(00H CHa Jo) Alkener veack utith Rypocmiorusacid Hoo *— oO eee ( Pow — hypoctlorus - 4 Ha Scho} HOT —> CHa Cita \ }) HU0.> thiorus oud, ae ae on W- . HU0 a> chloric aud nut cats Mor tite . r yor uaty vu tale a who u MIE puuktorc ; wou part los 4 ond ; a ir eqcewar cu aca 4 poly > aa a Strong : coe ‘ \ 7 FIO>PN OK ‘ “ ow / u 7 act with Wot! lO3 +0 ; | Fornad predua rel que dol eq CHa CHa 4 Wayico; 1 7 ow & (0) _Podyniun after — stun Jorge no. ol, small moktuutts a big MOLLE Called poly’ oust avid dhe se CH ta FN FOOD iN \ ] J OW ov Hw Covabdiwu 40 form amd smalun mola PuoUsH wow phunowuna Js frou as padyrstratiort Nigh iere fore onae om (An = CHa Tage poe ssi Poly tute” S ; ite MDP CHgh Aunt Y Poupl rune) A Akkyru Or vie tna tet eo Uvsalimatid beiple bonded hycioccubons - 8 Gcnmal {or 6 ¢ ie 4g formauia (CrHon-a) . cs (esan ) | m=2 Co Ha ethyne Cac (acetylene) nes Cana propyre Pre : ° , tepmatren of AlKYMES* — Hy drodysis ef Casbi cls eee Lats) 10 Pct — ey Bere —— ® Hy dstodusic ef Cala Jo qi auty Wine exe on + a Cad + ——> jy t caconda C(m___-H OH ca @) Mydiatysie of male 40 gue pwopyne - Mqala t+ Heo ——sS ch,-C=CH + Mqcor) a \m Pp ib ice) 40 qiut metho! @ Hidrorysic of Are AL, Cs CALLUMELCLUN COs Ah4(a 4.12 H20 ~ > 4 ALCOW), 4 2cHa - Sn 12 OH A Nuydrowysie Of cic Fo qeue methane — aa Fa HO —> Si Cond, + CHE ee 4 Sau atid P @ ee of uidnal da palide ~ att of € wy 3 “ gavon UO eyecr 4 KBe 4 antsd ' 1 \ ’ \ By (By vot \ ‘Rt Monohauds tlio FOM a thene Dihatids alto KOM gepyme @) Fotbe Sleckrodytee Meth Metwod ag: Polos Matte (4 Coal ) k a ch — wo cH ~COOk muah H— COO” :° Wcek ST i 1 3 c cH — COO” => = aHao “= Ht+ 20H7 Aad anods - cyt coo i ee _ ce ti acOa ae cH (00 cH AA cathode aut 4 ae > Ws T° (S) Wlovotorm veadd with Cihuu CAQ) mu al as al ax CHUS form fem 1 engl B o-OW — CHE CHA GAQU Phosquee esarel u uct stearqas CU Noa ‘ = a Lang hing gos N30 > dtu, —249 ech 16 Ag ll Powder Prysicol “Propwdin ol Alkyne ° 41 4s move polar and mote reactive duel precen’ el two 7” bonds "AV behauws as electron source and add acked by elect 0 phiite uvatead ) Py O pasts Wy Aadic Natutve + - pay metal —> Saud Het ) ) ) ? eA oe Pvdi ogeh, The hyduogen directly aHatched 10 en, Nitvegen . —C= cyviple bond carbon ) > When ferminad alkynes veact with sodium metal 9 OY Sodemmide -jo for sate > CEcHINE— CECH CHa o CH 20 Rages CNa 4 NHH3 — CE CHINES 6 Sodium = Ade His mot Mely rcs behaviow divetily Ctermenal) attach to tHe cH y tava = Na C=¢-Nat Ht2 Audie belewious = “disodium a " aubyude . _? cedlu ussptid Sua with ateys Hauide 4° {orm » Lat gut atk YY Gus. How Ut you conuut 7 Yell we 4o Pvopym’ = (CHE CH) CHEC q Ha Ge CHE C-CHR DE phayne 4O bubyne — . CHE CH 4 NaNH, ——S(H= ile eee ey | 3) Eikyne to Bul ae yne (HEH) (CH=CH) : acH -& CWECh 4 aNa ——s Noct= (-Na—_—> Me 5 5 4 QNaU' @ Hydrotysie Of Alkymes © — (Husssoplaitic ada” vu) > Im Precence of diktcke H> S04. and Hqso4 40 form aldehyde o1 fetone - cac-Ctk, ‘ | \ eqs CHE CH 1 Ho wat eset GH =CH peanamge mek ‘ wt aot | CHa-CH=0 ov ethanal 4 oH eter (OH new ‘ . SJable on double bord ) ' 4 i < feq CH3- CECH 1 Hoo WOES Cha C= Hy a HE Wu . o# of OH” Ausone * 4 propamone | eeWsrcH= C= ¢- Cy ets yy ch fee CHS | 2 CHa. ‘ cha OW 3) Reaction with Arsenic (hlovidy — co Ghia ; CAs ) CH, 0 CHE CH—=> (HECH 4 ASU ——> (HE cH \ \ a ASUT .! ? Luusite (polgnout aus)

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