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In the hydrolysis of bromoethane by aqueous sodium hydroxide, what is the nature of the attacking group and of the leaving group? | attacking group | leaving group | |-----------------|---------------| | A | electrophile | | B | electrophile | | C | nucleophile | | D | nucleophile | - CIE - A-Level Chemistry - Question 25 - 2014 - Paper 1

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In-the-hydrolysis-of-bromoethane-by-aqueous-sodium-hydroxide,-what-is-the-nature-of-the-attacking-group-and-of-the-leaving-group?--|-attacking-group-|-leaving-group-|-|-----------------|---------------|-|-A---------------|-electrophile---|-|-B---------------|-electrophile---|-|-C---------------|-nucleophile----|-|-D---------------|-nucleophile----|-CIE-A-Level Chemistry-Question 25-2014-Paper 1.png

In the hydrolysis of bromoethane by aqueous sodium hydroxide, what is the nature of the attacking group and of the leaving group? | attacking group | leaving group ... show full transcript

Worked Solution & Example Answer:In the hydrolysis of bromoethane by aqueous sodium hydroxide, what is the nature of the attacking group and of the leaving group? | attacking group | leaving group | |-----------------|---------------| | A | electrophile | | B | electrophile | | C | nucleophile | | D | nucleophile | - CIE - A-Level Chemistry - Question 25 - 2014 - Paper 1

Step 1

attacking group

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Answer

In the reaction involving the hydrolysis of bromoethane with aqueous sodium hydroxide, the attacking group is the nucleophile. Hydroxide ions (OH-) act as the nucleophile and attack the carbon atom bonded to the bromine in bromoethane.

Step 2

leaving group

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104 rated

Answer

The leaving group in this reaction is bromide (Br-). Bromine is a good leaving group due to its ability to stabilize the negative charge after departing from the substrate. Thus, during hydrolysis, the bond between the carbon and bromine breaks, allowing the nucleophile, hydroxide, to bond with the carbon.

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