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  • Dahyd: Cpymdine

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    1. A mixture of aniline and anisaldehyde is heated with sulfuric acid to form quinoline in a mild oxidation reaction catalyzed by pentoxide. 2. Furfural can be prepared by dehydration of pentoses like xylose with mineral acids. It can also be prepared by decarbonylation of furoic acid with sulfuric acid. 3. Thiophene can be prepared by heating 1-butene with sulfur at 650°C or by distillation of furfural with barium sulfide.

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    1. A mixture of aniline and anisaldehyde is heated with sulfuric acid to form quinoline in a mild oxidation reaction catalyzed by pentoxide. 2. Furfural can be prepared by dehydration of pentoses like xylose with mineral acids. It can also be prepared by decarbonylation of furoic acid with sulfuric acid. 3. Thiophene can be prepared by heating 1-butene with sulfur at 650°C or by distillation of furfural with barium sulfide.

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    5 views4 pages

    Dahyd: Cpymdine

    Uploaded by

    Sharp Pilot
    1. A mixture of aniline and anisaldehyde is heated with sulfuric acid to form quinoline in a mild oxidation reaction catalyzed by pentoxide. 2. Furfural can be prepared by dehydration of pentoses like xylose with mineral acids. It can also be prepared by decarbonylation of furoic acid with sulfuric acid. 3. Thiophene can be prepared by heating 1-butene with sulfur at 650°C or by distillation of furfural with barium sulfide.

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    of 4

    Paepaiation with

    uoith Conuntsatad
    conuntatad
    Pîpeudine

    6 dahyd bgenatioo nitobin-yena o t


    with
    300
    dulphusic axid at

    Conc. H2 So4
    3H2

    CPymdine
    H
    Cptpoidina)
    dichlororyethana
    in PrANCe
    uuth
    Pvuola
    2 By heaking
    dodium Qnthoido

    +CHL2 2c, HsO Na +2 Nacl+

    CPyridina) 2CHOH

    Pnel)
    suB coDE :
    REGNO: II520203o01 CY 821
    NAME A.AHAMED HUNAIF Sue NAME: ORGAPNIc
    CHEMISTPY

    D Quinolin
    e kRaup thariu
    A mixtwa e aniune and a n a l

    aatad in duuphunic atd and


    peseno e
    uwally nikroemgra e
    a mild oidising ayent
    the
    JOtion 2othamic
    auseni Pentoxido .

    and tends dto beLom vioonk


    acid s addid to meaka
    dulpha ol berit
    acion itlord
    tha
    CH OH
    Cone.F2S0p

    CHOH

    NH2 CeH NOA


    CH0H
    (ani ine)
    Colyca quinoine)

    (29 By Piediandas dynthuis Th invoves Tne


    **

    tondanbakion e 0- amäno bengaldehyda with aataldskyde


    PrAJnte
    alkali

    +2H2o
    NH H

    O Aminoberhal- A kaldahgde uinokure)


    dahyda

    DATE g.no SignkUre


    i P1apaaton

    tunal
    with pottasiusm ditromota
    Oidotiun et
    auwauent dacadouotisn
    uoic aid and

    200 3ooc
    at
    -
    .

    +Coj
    H
    .

    K2CT20H4
    fD (fisan
    FuLynal)
    uual dtream nthe
    By dacastbonlation o
    (2
    ie oide Cakaluk
    Proen e
    Ag.0 +Co
    C H Steam

    (furan
    Cutnal)
    e

    DATEF Pa.no Signatuse


    civPrarazattn

    aid wth bauim


    weic
    By distilation o
    B
    dulphid
    citil
    OH +Bas +Ba 3

    fwror aid) CThiophane)

    n - butana
    in t h
    &ulphuL wth
    2 B8abios
    ds pha at 650 c

    H2C CH2 650


    +4s t+3H,S
    HaC CH
    thiophare)
    (n-butan)

    DATE Pg.no Signaayge


    22/02/2022

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