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blsea [12.9K]
4 years ago
12

Please help me, I am confused on this.

Chemistry
2 answers:
weeeeeb [17]4 years ago
4 0

Answer:

The First choice is correct

Explanation:

That is the closest example of what is shown

Sophie [7]4 years ago
4 0

Answer:

A

Explanation:

Makes the most scene

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Which set of procedures and observations indicates a chemical change?
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Option 4 seems to be the one undergoing a chemical change because there is a formation gas from the bubbling that occurs. Chemical change is the change that results to the formation of a new substance. The other options given are examples of physical change.
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Which of the following is true of an effective scientific model?
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What is a concussion, and how is it related to force?
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6 0
3 years ago
What is the main side reaction that competes with elimination when a primary alkyl halide is treated with alcoholic potassium hy
Elanso [62]

Answer:

The main competing reaction when a primary alkyl halide is treated with alcoholic potassium hydroxide is SN2 substitution.

Explanation:

The relative percentage of products of the reaction between an alkyl halide and alcoholic potassium hydroxide generally depends on the structure of the primary alkylhalide. The attacking nucleophile/base in this reaction is the alkoxide ion. Substitution by SN2 mechanism is a major competing reaction in the elimination reaction intended.

A more branched alkyl halide will yield an alkene product due to steric hindrance, similarly, a good nucleophile such as the alkoxide ion may favour SN2 substitution over the intended elimination (E2) reaction.

Both SN2 and E2 are concerted reaction mechanisms. They do not depend on the formation of a carbocation intermediate. Primary alkyl halides generally experience less steric hindrance in the transition state and do not form stable carbocations hence they cannot undergo E1 or SN1 reactions.

SN2 substitution cannot occur in a tertiary alkyl halides because the stability of tertiary carbocations favours the formation of a carbocation intermediate. The formation of this carbocation intermediate will lead to an SN1 or E1 mechanism. SN2 reactions is never observed for a tertiary alkyl halide due to steric crowding of the transition state. Also, with strong bases such as the alkoxide ion, elimination becomes the main reaction of tertiary alkyl halides.

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3 years ago
What does molecule mean?
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Read 2 more answers
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