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    Organic Chemistry Ii: Experiment No. and Title

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    Fatimah Azzahrah
    SIR HAFIZ Aim: To synthesise 2-bromo-1-phenylethanol from styrene oxide and hydrogen bromide. Theory: Styrene oxide is an epoxide that can undergo nucleophilic substitution reactions. When reacted with hydrogen bromide, the bromine ion will attack the less hindered carbon of the epoxide ring, resulting in ring opening and formation of 2-bromo-1-phenylethanol. Procedure: 1. Styrene oxide (10mmol) was added to a round bottom flask and dissolved in dichloromethane (20mL). 2. Hydrogen bromide (48% w/w

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    Organic Chemistry Ii: Experiment No. and Title

    Uploaded by

    Fatimah Azzahrah
    26 views1 page
    SIR HAFIZ Aim: To synthesise 2-bromo-1-phenylethanol from styrene oxide and hydrogen bromide. Theory: Styrene oxide is an epoxide that can undergo nucleophilic substitution reactions. When reacted with hydrogen bromide, the bromine ion will attack the less hindered carbon of the epoxide ring, resulting in ring opening and formation of 2-bromo-1-phenylethanol. Procedure: 1. Styrene oxide (10mmol) was added to a round bottom flask and dissolved in dichloromethane (20mL). 2. Hydrogen bromide (48% w/w

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    chemistry

    Original Title

    C.V CHEM 310

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    SIR HAFIZ Aim: To synthesise 2-bromo-1-phenylethanol from styrene oxide and hydrogen bromide. Theory: Styrene oxide is an epoxide that can undergo nucleophilic substitution reactions. When reacted with hydrogen bromide, the bromine ion will attack the less hindered carbon of the epoxide ring, resulting in ring opening and formation of 2-bromo-1-phenylethanol. Procedure: 1. Styrene oxide (10mmol) was added to a round bottom flask and dissolved in dichloromethane (20mL). 2. Hydrogen bromide (48% w/w

    Copyright:

    © All Rights Reserved
    Download as DOCX, PDF, TXT or read online from Scribd
    Download as docx, pdf, or txt
    26 views1 page

    Organic Chemistry Ii: Experiment No. and Title

    Uploaded by

    Fatimah Azzahrah
    SIR HAFIZ Aim: To synthesise 2-bromo-1-phenylethanol from styrene oxide and hydrogen bromide. Theory: Styrene oxide is an epoxide that can undergo nucleophilic substitution reactions. When reacted with hydrogen bromide, the bromine ion will attack the less hindered carbon of the epoxide ring, resulting in ring opening and formation of 2-bromo-1-phenylethanol. Procedure: 1. Styrene oxide (10mmol) was added to a round bottom flask and dissolved in dichloromethane (20mL). 2. Hydrogen bromide (48% w/w

    Copyright:

    © All Rights Reserved
    Download as DOCX, PDF, TXT or read online from Scribd
    Download as docx, pdf, or txt
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    ORGANIC CHEMISTRY II

    Experiment No. and Title :

    Date of experiment:

    Group: A4AS1204_C

    Lecturer :
    SIR HAFIZ

    No. Name of Students Student No.


    1. Nursyazana Binti Faharul Radzi 2015384017

    2. Fatimah Azzahrah Binti Azizan 2015541881

    3. Rabiatulaina Binti Ramly 2015114907


    4.
    5.
    6.

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