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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
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
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