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BaLLatris [955]
2 years ago
15

Plan an investigation to explore the relationship between properties of substances and the electrical forces within those substa

nces.

Chemistry
1 answer:
kenny6666 [7]2 years ago
8 0

Answer:

la verdad no se no ablo ingles solo espanis

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What is the pH of a 0.028M solution (pH= -log(M))<br><br> A) 3.56<br> B) 2.88<br> C) 1.55<br> D) 1
kupik [55]

Answer:

1.55

Explanation:

-log(M)=pH

- Hope that helps! Please let me know if you need further explanation.

4 0
3 years ago
Copy the lists of measurements shown below. Pay close attention to the units that follow each number. List 1: 150 mL 11 mL 200 m
stich3 [128]

a) cross out 11mL from list 1, 2 mL from list 2, and 998 cm3 from list 3.

b) circle 200 mL from list 1, 801 mL from list 2, and 1 L from list 3.

7 0
2 years ago
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Someone please help me I will give BRAINLIST
blsea [12.9K]
  1. b
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  3. e
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3 0
2 years ago
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What is 2n^2 rule ( of science)​
lozanna [386]

2n² rule:

This rule is used to determine number of electrons in particular shell.

n=1 means K shell

n=2 means L shell

n=3 means M shell

n=4means N shell

The first K shell can hold upto 2 electrons, L shell can hold up to 8, third M shell can hold up to 18and the fourth N shell can hold upto 32 electrons. This rule of arrangement of electrons according to the shell is known 2n2 rule where n means number of shell.

For example: There is one proton in the nucleus of hydrogen atom, which moves in K shell path. It has no neutron.

3 0
3 years ago
Which of the following alkyl halides will react fastest with CH3OH in an SN1 mechanism?
yaroslaw [1]

Answer:

IV

Explanation:

The complete question is shown in the image attached.

Let us call to mind the fact  that the SN1 mechanism involves the formation of carbocation in the rate determining step. The order of stability of cabocations is; tertiary > secondary > primary > methyl.

Hence, a tertiary alkyl halide is more likely to undergo nucleophilic substitution reaction by SN1 mechanism since it forms a more stable cabocation in the rate determining step.

Structure IV is a tertiary alkyl halide, hence it is more likely to undergo nucleophilic  substitution reaction by SN1 mechanism.

5 0
3 years ago
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