A small amount of another organic product is formed in a Williamson ether synthesis. What is this product when the alkyl halide used in the synthesis of butyl propyl ether is
a. propyl bromide?
Verified step by step guidance
1
Identify the main reaction: The Williamson ether synthesis involves the reaction of an alkoxide ion with an alkyl halide to form an ether. In this case, the desired product is butyl propyl ether.
Consider the side reaction: In Williamson ether synthesis, an elimination reaction can occur as a side reaction, leading to the formation of an alkene.
Determine the alkyl halide: The alkyl halide used is propyl bromide (C3H7Br).
Identify the possible elimination product: The elimination of HBr from propyl bromide can lead to the formation of propene (C3H6).
Conclude the side product: The small amount of another organic product formed is propene, due to the elimination reaction of propyl bromide.
Recommended similar problem, with video answer:
Verified Solution
This video solution was recommended by our tutors as helpful for the problem above
Video duration:
3m
Play a video:
Was this helpful?
Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Williamson Ether Synthesis
Williamson ether synthesis is a method for creating ethers through the reaction of an alkoxide ion with a primary alkyl halide. This reaction typically involves nucleophilic substitution, where the alkoxide acts as a nucleophile, attacking the electrophilic carbon of the alkyl halide, resulting in the formation of an ether and a halide ion.
Alkyl halides are organic compounds containing a carbon atom bonded to a halogen atom (such as bromine, chlorine, or iodine). In the context of Williamson ether synthesis, the choice of alkyl halide is crucial, as primary alkyl halides favor the desired nucleophilic substitution reaction, while secondary or tertiary halides may lead to elimination reactions instead.
In organic reactions, side products can form alongside the desired product due to competing reaction pathways. In the case of Williamson ether synthesis, when using propyl bromide, a common side product is the formation of propene through elimination, especially if the reaction conditions favor this pathway. Understanding these side reactions is essential for predicting the outcome of the synthesis.