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nalin [4]
3 years ago
5

6. What do the data tell you about your hypothesin?

Chemistry
1 answer:
Vikentia [17]3 years ago
8 0

Answer:I like cheese

Explanation:do you like cheese

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cricket20 [7]
You should give a picture of the fable!
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Why do cells have a plasma membrane
ruslelena [56]
To protect foreign objects from entering...
8 0
3 years ago
A gas has a volume of 1.50mL at 1.89atm. What is the volume when the pressure is 2.75atm? What is the name of the gas law used t
ValentinkaMS [17]

Explanation:

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7 0
3 years ago
Predict whether or not a precipitate forms upon mixing 175.0 mLmL of a 0.0055 MKClMKCl solution with 145.0 mLmL of a 0.0015 MM A
Lorico [155]

Answer:

AgCl

Explanation:

The reaction of KCl (In aqueous phase K⁺ + Cl⁻) with AgNO₃ ((In aqueous phase Ag⁺ + NO₃⁻) produce:

Ag⁺ + Cl⁻ ⇄ AgCl(s)

The reaction has a k of 5.56x10¹⁰

That means you will produce 5.56x10¹⁰ molecules of AgCl per molecule of Ag⁺ and Cl⁻ in solution.

As the AgCl is in solid state, this molecules is the precipitate.

I hope it helps!

4 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.

7 0
3 years ago
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