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  • Aldehyde Ketone Carboxylic Acids

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    Janhavi Sahu
    5 views8 pages
    The document discusses several chemical reactions and syntheses. It describes processes for converting ketones and acids to other compounds using reagents like palladium, barium sulfate, quinoline, and xylene. Reduction and oxidation reactions are performed using reagents like hydrogen gas, nickel, palladium, and lithium aluminum hydride to reduce carbonyl groups or convert alcohols to alkanes. Compounds are also synthesized through acid-base reactions, hydrolysis, amination, nitration, and halogenation reactions.

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    The document discusses several chemical reactions and syntheses. It describes processes for converting ketones and acids to other compounds using reagents like palladium, barium sulfate, quinoline, and xylene. Reduction and oxidation reactions are performed using reagents like hydrogen gas, nickel, palladium, and lithium aluminum hydride to reduce carbonyl groups or convert alcohols to alkanes. Compounds are also synthesized through acid-base reactions, hydrolysis, amination, nitration, and halogenation reactions.

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    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Flag for inappropriate content
    5 views8 pages

    Aldehyde Ketone Carboxylic Acids

    Uploaded by

    Janhavi Sahu
    The document discusses several chemical reactions and syntheses. It describes processes for converting ketones and acids to other compounds using reagents like palladium, barium sulfate, quinoline, and xylene. Reduction and oxidation reactions are performed using reagents like hydrogen gas, nickel, palladium, and lithium aluminum hydride to reduce carbonyl groups or convert alcohols to alkanes. Compounds are also synthesized through acid-base reactions, hydrolysis, amination, nitration, and halogenation reactions.

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    © All Rights Reserved
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    of 8

    .

    Ketone And
    Aeid

    K,Ong01/

    (Rtoco),Ca+(Hecoj,ta
    R-CHoOH 0 A¡. 25o'e,
    pd- BaSOu
    Quineline
    H,Xyler (t4)
    n) 4g0/4

    Anay Alel, Hz0

    Col
    Ha/ Pd-Basoy

    Mmo S00°c

    ) (CH2)eN

    ) Sml/Cone Ho!
    ) dil H
    Cu/900'e

    Mmo300'

    CH,-=CH

    CH-HH
    K2 i,07/H,SO4

    ) 02,AaoH

    Cono H2So4

    + anhy
    Alel3

    anhy Alela A +

    s, Solvet,4

    Na HS03
    e=o +R-MqrA
    ethr Hol

    PTS

    Ha

    =0 + NH,OH

    NH 2

    2,4- bNP

    HCHO + NHg
    audalion

    Tllen's reagent

    Kg ,07/
    Cone H, 304

    Reduetion
    Ha/Pt oR
    Ha/Ni OR
    =0 H, /Pod
    LiAM

    /Core H

    OR Red P/Cora HI

    Rm- Hq/ore Hel

    LiALH
    l(e),eno], A

    il NacOH
    CHHO

    Ba (oH)e

    50. NaoH

    HOHO t
    50 KOH

    I0. NaoH

    Nao A
    l40
    dil
    ethanoi

    OH
    I0 NaoH

    Acid
    Carnboic H

    R CoOH

    NH3

    Pls oR So d2
    R- CoOH

    8,/cely

    Red (l
    H20/+

    eH,0H
    KMm O 4

    allalne
    allaline
    KMnoy
    KMmOy

    e
    llaline
    KMmoy

    alalne KMmoy

    coCHg
    ) I,/Aao)
    ) dil Hl

    ethr
    dy
    dil
    Hel
    Sodalime

    PCls 0R Socl,

    Cone H, SO, /Cane

    Bt, /FeBrg

    NH3

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