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    Diazonium Salt Easy To Understand

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    udhayadeepak60
    Diazonium salts are highly reactive compounds that decompose at high temperatures. They can be prepared by diazotization which involves treating an amine with sodium nitrite and hydrochloric acid. Diazonium salts are colored, crystalline solids that are soluble in water and decompose at their melting point. They undergo various substitution and coupling reactions like Sandmeyer reaction, Gattermann reaction, and Balz-Schiemann reaction.

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    Diazonium Salt Easy To Understand

    Uploaded by

    udhayadeepak60
    5 views4 pages
    Diazonium salts are highly reactive compounds that decompose at high temperatures. They can be prepared by diazotization which involves treating an amine with sodium nitrite and hydrochloric acid. Diazonium salts are colored, crystalline solids that are soluble in water and decompose at their melting point. They undergo various substitution and coupling reactions like Sandmeyer reaction, Gattermann reaction, and Balz-Schiemann reaction.

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    Diazonium salt easy to understand

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    Diazonium salts are highly reactive compounds that decompose at high temperatures. They can be prepared by diazotization which involves treating an amine with sodium nitrite and hydrochloric acid. Diazonium salts are colored, crystalline solids that are soluble in water and decompose at their melting point. They undergo various substitution and coupling reactions like Sandmeyer reaction, Gattermann reaction, and Balz-Schiemann reaction.

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    © All Rights Reserved
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    5 views4 pages

    Diazonium Salt Easy To Understand

    Uploaded by

    udhayadeepak60
    Diazonium salts are highly reactive compounds that decompose at high temperatures. They can be prepared by diazotization which involves treating an amine with sodium nitrite and hydrochloric acid. Diazonium salts are colored, crystalline solids that are soluble in water and decompose at their melting point. They undergo various substitution and coupling reactions like Sandmeyer reaction, Gattermann reaction, and Balz-Schiemann reaction.

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    of 4

    MI W

    Page No

    Date:

    Diazoaium Salta
    *1'-amines ’ foun Aighly oatabde alkyldiazonium sot
    QAeneciaznum salts

    at lou tenperatuse,

    Pruparation Diazorin Colarz


    + NaNO, + HU 273 +AlalL t AHaO

    Tmp à maintaind sincL


    mt diazenwmsalts
    decompee at high tumpuatuue
    Beozene diazm umsalk
    (Diazotisatier)

    Phynial Praputis
    * ColDles, cnystalline
    * SoluLde in HaD
    Dompae at dy state

    Chemial Reatias:

    (Diazoy Laavig giaup


    ci tlalide s Cyande group
    Natx lul.
    H
    Luala
    HEH
    Lew) lats -BH
    HBH
    HeN

    Sandmayet Reactier) Cbtattemaan Reaction)


    Bttin gyuild.
    n aro
    n ef o r e
    M
    Page No.
    carbo
    Date:

    tit) Tadide ien:

    cal
    ti
    ert
    (ElueplDAi)
    audl (PPt)
    (Balz-schumaonHLatioo)

    HaPDs

    +cHaLHaDH CHa CHO

    + HaQ

    NaNe
    lpcasal)
    ChHs NEN-
    -NH2 -DH
    CH3
    N
    HT
    w
    ene)
    cp-amaDAZO
    fpinydaaglenzen)
    Page
    OH
    OH
    Examplas- NEN
    NEN
    Gulsstikution)
    Eutsaphilie Cupling
    =N-AM) -NCAH Amines diazoniumsolk.
    compouods Azo Phenetsl Benzne
    REACTIDN] coUPLIN
    group Dazo Runkien LB)
    Uare
    No. Page
    MT W T F S s
    Page No.:

    Date

    NENC

    NH2

    fp-aminophool)
    N=N-GHs W=N-laHe
    NH ceiha)
    (Osthol
    NH

    Reductio0
    NH-NHe
    N'ENLL
    Solel
    HL LPhunyt hydauie )

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