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emmasim [6.3K]
3 years ago
7

Will give brainliest

Chemistry
1 answer:
slamgirl [31]3 years ago
3 0
I will help you with answering this question.
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Im chemistry we are solving chemical reactions and on the assignments our teacher put the questions as riddels and I can not get
lara31 [8.8K]
Are they trying to be funny about it?
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Energy is transferred thru heat by each of the following methods EXCEPT?
Softa [21]
It doesn't transfer through Thermalizing
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2 years ago
Read 2 more answers
Calculate the pH at of a 0.10 Msolution of anilinium chloride . Note that aniline is a weak base with a of . Round your answer t
notsponge [240]

The question is incomplete, here is the complete question:

Calculate the pH at of a 0.10 M solution of anilinium chloride (C_6H_5NH_3Cl) . Note that aniline (C6H5NH2) is a weak base with a pK_b of 4.87. Round your answer to 1 decimal place.

<u>Answer:</u> The pH of the solution is 5.1

<u>Explanation:</u>

Anilinium chloride is the salt formed by the combination of a weak base (aniline) and a strong acid (HCl).

To calculate the pH of the solution, we use the equation:

pH=7-\frac{1}{2}[pK_b+\log C]

where,

pK_b = negative logarithm of weak base which is aniline = 4.87

C = concentration of the salt = 0.10 M

Putting values in above equation, we get:

pH=7-\frac{1}{2}[4.87+\log (0.10)]\\\\pH=5.06=5.1

Hence, the pH of the solution is 5.1

8 0
2 years ago
Compound A and compound B are constitutional isomers with molecular formula C3H7Cl. When compound A is treated with sodium metho
mars1129 [50]

Answer:

Compound A and compound B are constitutional isomers with molecular formula C3H7Cl.

When compound A is treated with sodium methoxide, a substitution reaction predominates. When compound B is treated with sodium methoxide, an elimination reaction predominates.

Explanation:

Constitutional isomers are the one which differs in the structural formula.

When compound A is treated with sodium methoxide, a substitution reaction predominates.

That means sodium methoxide is a strong base and a strong nucleophile.

But when it reacts with primary alkyl halides it forms a substitution product and when it reacts with secondary alkyl halide it forms mostly elimination product.

The reaction and the structures of A and B are shown below:

3 0
3 years ago
Speed.
Alexus [3.1K]
Increases with

hope this helped :))
correct me if i’m wrong
5 0
2 years ago
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