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    Hydro Fo My Lation

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    Usha gowda
    This document discusses the hydroformylation of alkenes to form aldehydes. The key steps involve: 1) Using a catalyst like cobalt or rhodium to add a carbon monoxide and hydrogen across the double bond of an alkene substrate, forming an aldehyde. 2) The reaction proceeds via an organometallic intermediate where the alkene binds to the metal center before the addition of CO and H. 3) The aldehyde product can then undergo further reactions like reduction to an alcohol or oxidation to a carboxylic acid.

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    Hydro Fo My Lation

    Uploaded by

    Usha gowda
    10 views8 pages
    This document discusses the hydroformylation of alkenes to form aldehydes. The key steps involve: 1) Using a catalyst like cobalt or rhodium to add a carbon monoxide and hydrogen across the double bond of an alkene substrate, forming an aldehyde. 2) The reaction proceeds via an organometallic intermediate where the alkene binds to the metal center before the addition of CO and H. 3) The aldehyde product can then undergo further reactions like reduction to an alcohol or oxidation to a carboxylic acid.

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    This document discusses the hydroformylation of alkenes to form aldehydes. The key steps involve: 1) Using a catalyst like cobalt or rhodium to add a carbon monoxide and hydrogen across the double bond of an alkene substrate, forming an aldehyde. 2) The reaction proceeds via an organometallic intermediate where the alkene binds to the metal center before the addition of CO and H. 3) The aldehyde product can then undergo further reactions like reduction to an alcohol or oxidation to a carboxylic acid.

    Copyright:

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

    Hydro Fo My Lation

    Uploaded by

    Usha gowda
    This document discusses the hydroformylation of alkenes to form aldehydes. The key steps involve: 1) Using a catalyst like cobalt or rhodium to add a carbon monoxide and hydrogen across the double bond of an alkene substrate, forming an aldehyde. 2) The reaction proceeds via an organometallic intermediate where the alkene binds to the metal center before the addition of CO and H. 3) The aldehyde product can then undergo further reactions like reduction to an alcohol or oxidation to a carboxylic acid.

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    © All Rights Reserved
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    of 8

    Hydoofoylatio

    Foromate of Ald enyde (AlNane t cot H


    Conmple

    Catalyst
    lo-yoB
    alReme Atdekgde. (haea)

    yamsned.
    Comutsin of alkaye to, alahy de
    he
    catey bydoofpnatboi
    Reachey

    C c bomd

    Co
    go-oc
    tivesvakihyde.
    Mechamiom
    'co,((olz

    CÓ
    Co.

    Co
    Co

    Co

    |18V6
    Reduche
    ALdeh de Triemsmethlato

    e16v6

    -ECO

    Addito
    tydoyamaho

    ene to
    to fovn Nitilk

    Sobstte = Akeme

    toper

    HCN
    CN

    Nie-ctelysd hydwgyunaton.

    hydriconÑe)

    athian hen

    oe mít ile.
    Lo
    HCN
    l
    onidaue As

    Redube H-Ni-L
    Nitile, 3. Elomheabon
    2

    cH..
    2.
    L.

    L.
    NiNim Som fatlyt
    Symoa chlorído -k-ýs (4-rphenglphspho)
    soletfve

    Lonypoumd

    Prhs

    su batrce - Aikene piodudajeaiie


    Compoynd

    Seleetu
    Sow ble im Beugane, Touleneo

    1.Ozbcdatu qddihay

    S.
    PPhs -H
    H Rh Rh H

    eehs
    icneae.
    as (u). in a mompob
    malede)

    2. |ANene Co-od asybeM

    a di hagto bomd wi (R)


    trbond)
    3. Miaten fmsewien)n
    ate settwa step.
    &<ow stp and hence

    4. Redoiue elianiation)

    . Akame
    SymnesiN

    RuoAc)e
    )-Bia
    (s- NAprogas.
    27-- ee

    2. Synmesin dibefra!

    Coot Cot
    (A)-Meo-BPHEP

    (Smibrdl.

    (caleim chenmmd blocu)


    Coot

    NAAC Aeo
    Ao

    BINOL-R

    ip,NET -’ í-isoprpeylonÛnt

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