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Organic AS 3

The document discusses the properties and reactions of halogenated alkanes, including their solubility and reactivity. It outlines various chemical reactions involving halogenated compounds, such as substitution and elimination reactions, and the conditions required for these reactions. Additionally, it touches on the mechanisms of these reactions and the influence of solvents on the reaction pathways.

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harram ahmed
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3 views11 pages

Organic AS 3

The document discusses the properties and reactions of halogenated alkanes, including their solubility and reactivity. It outlines various chemical reactions involving halogenated compounds, such as substitution and elimination reactions, and the conditions required for these reactions. Additionally, it touches on the mechanisms of these reactions and the influence of solvents on the reaction pathways.

Uploaded by

harram ahmed
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF or read online on Scribd
sahilog teed leone od ‘ alcone Fidegen auinvalives q Replacement of me or ne "HY alee 7 ay alia ans the aeipedlina halonen ~cbrinelive Sen dermal = Femnetarnale Group Cig KX MG Ovens Phen 21525334. Alam ei see Aarvelive® .~ ot Alicames —> with Subsliluentg — Aye (CR) Cy Cu (Bx) CH(CH — Pg &/ oe 08 @e 4- bromo —2-Chino ~#-metdl hesamne « CQ BY Ciao Papen $1 &- & &- CH CQ vo CHO CR : Ls pps poe = Ly papa foe a ? = a. i capac PAA Sa.9d fore @ “ela Halegeno alkanes have. 0 Ton ard THs tre Pesadk Ee hycaacaneors a cempanndnie. "WH thes “ due oe nh Polarity ° eK bend | which yeaa fo shoq PA- pA Paes betwen thecy molecular Hence eentidtnable — amount meng) “« feeuired — T ovencemne. aut pres. cy folubi Li pa ” Hal oe alkaneh hale pa pot wc are. not San frag Cs form wn bends with “3 , hence ane: ohe me Soluble m HO Thai Solu} Ai fovan — deveases ty neeting "heytopisete nit” In oleae, H, aroprobic unit - Chiro atkones are ete Romsey than C7) Dens WOO tha, Bloch mven tao. Sura ae HOY wWheroad te | aRecking Sucleopuite Lv. hatayen alm “‘ “exch bs atlases nucleo, ue) which ——-yedulls bn “Nucte optobc Swostitution iS eatin Now Sheng ob CX bn decesser down me mr og So a hon not y raatiey cnurmloey 4 Sheu. 2 Reactim with KOH — ow NaOH .- “ @) (2v) Reagents = OH” ae Heat /reptes. ond Conditions ey & c on - CH + On > CH cH OH - + 2CR By CQ = ou On a + 20H" 5 PI a BC Reackiom with AIA (formatcon a ome) Reagent = AH, of Chama ie Ammania - gi a AION 5 CR Sn i IP Malogeno alitone :- Of Halogen alan i bended fe Prima Corbkm alum, ten it is Caled [P= halogens alkane and Cb = 8 Catleon elem, which inet bonded Ur ~o ome Cartoon aLern oe mo CS. alm, CH - CH CQ Pe dalippooatns “ 2 }= A-ch o “ Gs wee - AR -CA a z / % 2 - hale. Alicomee = “f halogen alm) i bardad with cri Carbon eben ten it Pia “alepproetbone. DR Corton alm whith i Riverily bmoteol i] A Carte akem Wh Livery Lanolaol Teo Wo omy C alime i eollad 2 Baron Tom Ce J HC CR-CH 1 —— 3 Bhat Blinc xo Sf halogen Alen bonded S Carer alam, ton i & Callecf 3- halojene Alicane, A Carken alam WOhicn ie aie erded tree C alam. ia Cable 2°- Carbm ale a Sn eye eure ce (nye cH CR Reackion L CR [OH = CH-OH + ick Aenee ; haifiggne HO? Def > Ho on. > HO-eH 4 k , von 2, Rake OC [eHc2] LOH] aa 32 Gako caliion Hs I- Hs cr) en SOY > 4e-%-OH a 2) aac = = Ree OC (S alicia} co ef \ SS ae PoR Note .- a» _ halogencalkane Com — exhibit ~~ bein Spyl and Spy wrechamuisms , Orn ic Acpencda on TR le ca Dror oH sp mon polar Bhertl « used, thon SN* mechanison becomes Pavouraitd bevouse wo Sunda Sehvent Parmalion thon “ENO -mechanion becomes “fowrounaie because 69 Leh Solvent malin °f Corocalion — is Ae ieulL city 3 f polar Solvent «4 wed then sfamalion ot Carvoocalion & favourable, So yy hk Case. Sy mechanism ill be Eliminalio VeacDion:= Reape ~ KOH ow AaeOH - BQ conditiond s- Meal / ap lu CH = OH +. OH SS He=CH,L HO a es (ale) a > a -F aX ~ ethent- Hoey 5 Ke met — CH HCH, bout -2 -ene - an PR 2 Hom CH CH Cp bul- I-!ne Wn MW 3B aUeenes hove frre bul— j-ene’ bud - L- ene. Bees bk 2- ome 5 Heat /vab lug =c—@r- — Ni be 4o- SHR sKON > No vealton 3 of (CHA Sugectxcidlee ~ CH-CQ, Do 7 & a rE LE, ce e py F< 1 c- C 4 FE f acy Five epithe & Brome alco > CHa

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