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nekit [7.7K]
4 years ago
5

Draw the alkyne formed when 2,3-dichloropentane is treated with an excess of strong base such as sodium amide.

Chemistry
2 answers:
Xelga [282]4 years ago
8 0
Hi! Thank you for posting your question here at Brainly. I hope I would be able to help you with my answer.

When an alkyne such as 2,3-dichloropentane is treated with excess sodium amide, a two-step elimination reaction will happen. The reaction would then yield the final product in the form of 2-pentyne. Its structure is shown in the attached image.

BartSMP [9]4 years ago
4 0

Answer: We obtain the alkyne 2-pentyne through E2 reaction mechanism.

Explanation:

Alkyl halides are compounds that contain a carbon chain in which one or more hydrogen atoms have been replaced by a halogen atom (F, Cl, Br, I) and are characterized by having halogen atoms in adjacent carbons. In the dehydrohalogenation the alkyl halide is reacted with a strong base. As a result an alkyne is obtained.

In this case we use sodium amide to favor the type E2 reaction mechanism (type 2 elimination) and we obtain the following alkyne:

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4 0
3 years ago
3.
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3 years ago
The solid anhydrous solid CoCl2 is blue in color. Because it readily absorbs water from the air, it is used as a humidity indica
MrRissso [65]

Answer:

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6 0
3 years ago
The barium isotope 133ba has a half-life of 10.5 years. a sample begins with 1.1×1010 133ba atoms. how many are left after (a) 5
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4 0
4 years ago
Read 2 more answers
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