Hizi ni athari za kuondoa maji (dehydration) kwa alkoholi, ambapo alkoholi hupoteza molekuli ya maji na kuunda alkene. Asidi ya sulfuriki iliyokolea na joto la 180^ huwezesha athari hii

Chemistry

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CH2=C(CH3)2+H2O\text{CH}_2=\text{C}(\text{CH}_3)_2 + \text{H}_2\text{O}

C6H5CH=CH2+H2O\text{C}_6\text{H}_5\text{CH}=\text{CH}_2 + \text{H}_2\text{O}

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Hizi ni athari za kuondoa maji (dehydration) kwa alkoholi, ambapo alkoholi hupoteza molekuli ya maji na kuunda alkene. Asidi ya sulfuriki iliyokolea na joto la 180∘C180^\circ\text{C} huwezesha athari hii.

1. Athari ya 2-methylpropan-1-ol:
CH3CH(CH3)CH2OH\text{CH}_3\text{CH}(\text{CH}_3)\text{CH}_2\text{OH} na H2SO4\text{H}_2\text{SO}_4 iliyokolea kwa 180∘C180^\circ\text{C}.

  1. Protonation ya kundi la hydroxyl na kuondolewa kwa maji huunda carbocation ya msingi.

    CH3CH(CH3)CH2OH→H+CH3CH(CH3)CH2OH2+→−H2OCH3CH(CH3)CH2+\text{CH}_3\text{CH}(\text{CH}_3)\text{CH}_2\text{OH} \xrightarrow{\text{H}^+} \text{CH}_3\text{CH}(\text{CH}_3)\text{CH}_2\text{OH}_2^+ \xrightarrow{-\text{H}_2\text{O}} \text{CH}_3\text{CH}(\text{CH}_3)\text{CH}_2^+
  2. Carbocation ya msingi hupanga upya kupitia hydride shift (mabadiliko ya hidrojeni) kutoka kaboni ya pili hadi kaboni ya kwanza, na kuunda carbocation imara zaidi ya tertiary.

    CH3CH(CH3)CH2+→1,2-hydride shiftCH3C+(CH3)CH3\text{CH}_3\text{CH}(\text{CH}_3)\text{CH}_2^+ \xrightarrow{\text{1,2-hydride shift}} \text{CH}_3\text{C}^+(\text{CH}_3)\text{CH}_3
  3. Carbocation ya tertiary hupoteza protoni kutoka kaboni iliyo karibu na kuunda alkene.

    CH3C+(CH3)CH3→−H+CH2=C(CH3)2+H2O\text{CH}_3\text{C}^+(\text{CH}_3)\text{CH}_3 \xrightarrow{-\text{H}^+} \boxed{\text{CH}_2=\text{C}(\text{CH}_3)_2 + \text{H}_2\text{O}}

    Bidhaa kuu ni 2-methylpropene.

    2. Athari ya 2-phenylethanol:
    Benzene ring- CH2CH2OH\text{CH}_2\text{CH}_2\text{OH} na H2SO4\text{H}_2\text{SO}_4 iliyokolea kwa 180∘C180^\circ\text{C}.

  4. Protonation ya kundi la hydroxyl na kuondolewa kwa maji huunda carbocation ya msingi.

    C6H5CH2CH2OH→H+C6H5CH2CH2OH2+→−H2OC6H5CH2CH2+\text{C}_6\text{H}_5\text{CH}_2\text{CH}_2\text{OH} \xrightarrow{\text{H}^+} \text{C}_6\text{H}_5\text{CH}_2\text{CH}_2\text{OH}_2^+ \xrightarrow{-\text{H}_2\text{O}} \text{C}_6\text{H}_5\text{CH}_2\text{CH}_2^+
  5. Carbocation ya msingi hupanga upya kupitia hydride shift (mabadiliko ya hidrojeni) kutoka kaboni ya benzylic hadi kaboni ya kwanza, na kuunda carbocation imara zaidi ya benzylic.

    C6H5CH2CH2+→1,2-hydride shiftC6H5C+HCH3\text{C}_6\text{H}_5\text{CH}_2\text{CH}_2^+ \xrightarrow{\text{1,2-hydride shift}} \text{C}_6\text{H}_5\text{C}^+\text{HCH}_3
  6. Carbocation ya benzylic hupoteza protoni kutoka kaboni iliyo karibu na kuunda alkene.

    C6H5C+HCH3→−H+C6H5CH=CH2+H2O\text{C}_6\text{H}_5\text{C}^+\text{HCH}_3 \xrightarrow{-\text{H}^+} \boxed{\text{C}_6\text{H}_5\text{CH}=\text{CH}_2 + \text{H}_2\text{O}}

    Bidhaa kuu ni styrene (ethenylbenzene).

    3. Athari ya 2-methylpropan-2-ol:
    (CH3)3C−OH(\text{CH}_3)_3\text{C}-\text{OH} na H2SO4\text{H}_2\text{SO}_4 iliyokolea kwa 180∘C180^\circ\text{C}.

  7. Protonation ya kundi la hydroxyl na kuondolewa kwa maji huunda carbocation ya tertiary.

    (CH3)3C−OH→H+(CH3)3C−OH2+→−H2O(CH3)3C+(\text{CH}_3)_3\text{C}-\text{OH} \xrightarrow{\text{H}^+} (\text{CH}_3)_3\text{C}-\text{OH}_2^+ \xrightarrow{-\text{H}_2\text{O}} (\text{CH}_3)_3\text{C}^+
  8. Carbocation ya tertiary hupoteza protoni kutoka kaboni iliyo karibu na kuunda alkene.

    Hakuna mpangilio upya unaohitajika kwani carbocation tayari ni imara.

    (CH3)3C+→−H+CH2=C(CH3)2+H2O(\text{CH}_3)_3\text{C}^+ \xrightarrow{-\text{H}^+} \boxed{\text{CH}_2=\text{C}(\text{CH}_3)_2 + \text{H}_2\text{O}}

    Bidhaa kuu ni 2-methylpropene.

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