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How do we convert Propan-1-ol to bromopropane? - Answers

To convert propan-1-ol to bromopropane, you can perform a nucleophilic substitution reaction using a strong acid, such as hydrochloric acid (HCl) or phosphorus tribromide (PBr₃). First, treat propan-1-ol with PBr₃, which will convert the alcohol into a bromide by replacing the hydroxyl group with a bromine atom. The reaction produces bromopropane as the primary product.



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How do we convert Propan-1-ol to bromopropane? - Answers

https://math.answers.com/math-and-arithmetic/How_do_we_convert_Propan-1-ol_to_bromopropane

To convert propan-1-ol to bromopropane, you can perform a nucleophilic substitution reaction using a strong acid, such as hydrochloric acid (HCl) or phosphorus tribromide (PBr₃). First, treat propan-1-ol with PBr₃, which will convert the alcohol into a bromide by replacing the hydroxyl group with a bromine atom. The reaction produces bromopropane as the primary product.



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https://math.answers.com/math-and-arithmetic/How_do_we_convert_Propan-1-ol_to_bromopropane

How do we convert Propan-1-ol to bromopropane? - Answers

To convert propan-1-ol to bromopropane, you can perform a nucleophilic substitution reaction using a strong acid, such as hydrochloric acid (HCl) or phosphorus tribromide (PBr₃). First, treat propan-1-ol with PBr₃, which will convert the alcohol into a bromide by replacing the hydroxyl group with a bromine atom. The reaction produces bromopropane as the primary product.

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      To convert propan-1-ol to bromopropane, you can perform a nucleophilic substitution reaction using a strong acid, such as hydrochloric acid (HCl) or phosphorus tribromide (PBr₃). First, treat propan-1-ol with PBr₃, which will convert the alcohol into a bromide by replacing the hydroxyl group with a bromine atom. The reaction produces bromopropane as the primary product.

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