Document Details

IndulgentTan7301

Uploaded by IndulgentTan7301

Tags

organic chemistry nomenclature chemical properties organic compounds

Summary

This document discusses various aspects of organic chemistry, including nomenclature and chemical properties of different compounds. It features structures, reactions, and concepts related to organic chemistry.

Full Transcript

④ 1,3, Thlaz've 31-1 Azepene - ÷a÷¥¥r Mm ÉÉK ---_ III most systematic nomenclature 4 3...

④ 1,3, Thlaz've 31-1 Azepene - ÷a÷¥¥r Mm ÉÉK ---_ III most systematic nomenclature 4 3 2 or 9- cyclo hexofz 5) Osca , diene ④ 3) diazo penta (2/4) diene l ' 2,3 - 9 4 z s I Pyrrolidine ' " 2- CHI - Ptdinnefqnmdlue 3,3 ,3 -1M Cyclopentadienyl anion in similar very chemical properties en. 82°C v6 few except → Bp , poop physicochemical Intermoleculbondar's → hydrogen ☐ " J an ;D formed 124°C are case this in -32°C 30 I ABMO I - - - -1 - - - - l BMO : neutral N' atom electrically ' Py sole charge on nuclear 92 OR higher ÉE - :& goes got yes it xp poor ° Boi go " a. & "" or 5T¥ " g. " " of " " E " " Sato ii gagamongn.ro ! → g. go.org g. " " & :* i i roses :* e. " - i.go.io.. I µ , ooÉ wife it RDS Benzene loosing aromaticity fast step Benzeneregains dog -11 aromaticity. e " ° sseacti as ciot¥dnP÷§ ¥ " pyrrole " safe , aid " Is pj%ge°É→! µ " 's - d or ÑÉ pierre ayy. ¥ , g. y # yes g- * opwoeoj.ae ooo goes " roé ✗ = 5 I of @ release ^ ↳ I effect al°+ extent +m , es cycles go yay we , Hoh " " wage K vetoed °& * & " gather µ , " " " case ,ggoÉ µ , in y * i , * ÷÷÷÷ reason eV¥É ^ , " peter o µ , , * amiral we ¥60T ' attack 's system " " " " w w.atfa.ofdedAP woot"" "".gg# case - it µ item w.gg , g. & t pm m Ms m as ) "" change separated resonance less stable ( un stsucfure far from + the (ii. , ") charge Negative change is too much distance coffee acyclic "%e sin from or it we d. -88 A JCCURAL ( s UUL LU LI / ( 011110 Ll / ( LL V1 LILL Llull 1 Lll get ootv pot # so I , s g is. ← % !@ § ↳ a 5 § ¥ good leaving group reaction vigorous conditions " probit completely zoned " partial. pedal - Ignore " ÷÷ a ' > nest soon i i 0i [email protected] to due → 126° * - - e- 3 : 2 :S :& Mann condensation N%dd → shift 's base generated in situ base → reaction shift electrophile dehydration in the g- as acts (prefect) duncfionadise rEÉ to easy → Pyrrole by using mannich reaction strong base > aromatic vetoes reacts;+h pymkweyag.pwd.igot o ' about azafrekienium cation (highly unstable) linear dinner gig :UM Pulver aza cation herd etoap + " ^ poopwf Feet on if pyrrole F-☐ better MAIL./gHd- to salt prep diazonium ÷÷:÷T ÷÷÷i÷. ,. good * gag ° g. story " µooHµ° I i 4 minor major HARE - - four of oxidation reactions of pyrrole types colourless stored in amber coloured bottle (cuz it easily undergo oxidation pyrrole - - " www..io ' ambient conditions ✗☒ radical reaction river µÉ¥%¥ÉÉ not major at generally ☒☒ dimer quasi radical 't " excessMatic " dd g. ago cÑ° & µ OPP solid mattered slightly strong heating method to miss :b/e with wateg goa dy distillation → pgp→Ñ° ° ← * - COOH g-cÉ° " while shutting the air off. distillation Ho - Yoon a°. shows Krah :S acid diffgac Spectra planar gaeacteo :c * chloroform like say me so Agzo odious @ hoon Mn 211+2504 4211-22 On - CHO ( 0 Goose) g.ir?** of orbital g. www.nn.y.gangf/ I more 's contributestability to less stable "catalyst Ago ÑÉ ÷ µ, of go → ÷ →¥0 , - ggrc } " " " ;÷÷÷÷Tt " r :* !÷ get"Ña*.iocure cast. g.gg/gi *÷÷ " g. ai.ir →;g÷pi.ee/g:or&Ggecofo0Mfa,..gcotabf& ggygg. g. r0°°°. of " :* R 0 CHO R 0 for heroin limitations of this process hindered di ketones resist formation of mono enol sterically - * mechanism follows by - reaction to undergo cyclisation rod acid?Ñ " gift µzcÑ pentoxide an pwsphpo ✗ - position ' ✗ - position of furan sing aekynylsulfoniumn salt di ketone p - NaOH Peo chloric acid aq C" & "@ even ↳ zeacti org more are neurone ESR war towards * ① ④ e- " But inpresence acid Ñ°& * → then - B se ¥¥ of takes place egged enhanced , gang ¥ , , e- og m > a÷ox - µ app *¥ ✓ 7 conditions mild É° under ignores g. is less obtained yield , , , , % - f- ketone :" e is opening degixat sing i. y giver acid w used occults acid is '" jyzat °P "7 * agents e ragegoing → if conc rid → so mild conditions Edd product 2,5 - " " "" * r÷ÉY µ ,.mn www..gg, y, , am , low % yeild used (oaceni cation) if sulfuric acid is it undergoes polymerisation or ping opening so it is not used (like pysaa) -40°C zs of reagent excess 6M g- " " " ↳actionodds resists " " " '°^ " it cat gone gum yyn.fi og f. see undergo.ir &. ,. g.. vi. temp room most prof at ered tent low at -80% yield is intermediate " " :# ° add poodle hnknd ehgbeaio.cat teiji.io 's mix of product Br exchange d- > tr chloro furan - tetra chloro furan t equate (minor ) - Iz Crajor guy of in equivalence of product 's change % yield changes EWG← 5- sub major e- nighter.fr top - * major - 3 ) otgd;¥p+ catalyst id Ifm Ceto high reactivity f- due to É - 2 : I Zak * dei:c.io F-ING easily al k yl a ted * *r - side mix of heroin methyl 2- double exocydia bond formed 100°C " " *°Ñ " oeacxi-i-tf.ir " * y acting of methyl substituted requires decreased conditions 200°C so halo furan is harsh Nac Sub possible 9 ENG Nuc sub facilitates mm fast so no addition product stable so add Product formed " " at sufis No radicals by ✓ carbene gives carbone gene major pundit "µ%e of. isomers but maleic be ☒ any stable Ealy kind - major maleamrde 1 wfoe * G- NÑ can be separated from each other moments due to different dipole Mf furan f alkene + alkene post major Fermat undergoesN" ii. " qq.mn. ← → " g.. se dielectric constant with water Colourless liquid b. p → 84°C benzene 80°C it's possible to separate miscible , } → so f- P→ -38°C → -3°C Thio → 16 being →2.2 thiophene by diff physical & many organic solvents methods contains impurities of thiophene cuz it is separated b.p distillation method Genz & thio are similar gut nor using to benzene physical properties similar chemical & a@ thiolin 2- thiolin 3- Resonance 29 34 kcal Imo I energy - → e- donated e- / @ acceptor metalation

Use Quizgecko on...
Browser
Browser