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AlexFokin [52]
3 years ago
15

Pls help i have no clue what the right answers are

Chemistry
1 answer:
Finger [1]3 years ago
7 0
Question 2: AuN3
question 3: NiBr3
question 4: CrP2
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Please help me ill give brainiest to the right answer
aleksley [76]

Answer:

D.

Explanation:

Cause the weather made those rocks. Like volcanos and weather.

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Why are valence electrons important?
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They are the outer layer of the electron layers.
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I NEED HELP ASAP !
Lana71 [14]

Answer:

1.

643.21g  1 mol  6.022^23

262.87 g   1 mol

= 1.4735E24     [Mg3(PO4)2]

2.

4.061x10^24          1mol                22.4 (L)  

6.022^23       1mol

= 151 liters H2O2

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479.3g   1 mol   6.022^23

18.02g    1mol

= 1.60E25 H20 atoms

4.

80.34L   1mol       164.1

22.4L       1mol

588.6g   Ca(NO3)2

5.

893.7g   1mol       22.4

44.01g   1mol

= 427 L CO2 or 427.4

6.

5.39 x 10^25     1mol     78.01

6.022^23    1mol

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hope this helps!! :)

8 0
3 years ago
The modern view of an electron orbital in an atom can best be described as
Roman55 [17]

Answer:

An orbital is a region in space where there is a high probability of finding an electron.

Explanation:

The orbital is a concept that developed in quantum mechanics. Recall that Neils Bohr postulated that the electron occupied stationary states which he called energy levels. Electrons emit radiation when the move from a higher to a lower energy level. Similarly, energy is absorbed by an electron to move from a lower to a higher orbit.

This idea was upturned by the Heisenberg uncertainty principle. This principle state that the momentum and position of a particle can not be simultaneously measured with precision.

Instead of defining a 'fixed position' for the electron, we define a region in space where there is a possibility of finding an electron with a certain amount of energy. This orbital is identified by a set of quantum numbers.

7 0
3 years ago
When comparing the two chair conformations for a monosubstituted cyclohexane ring, which type of substituent shows the greatest
Aleksandr [31]

Answer:

See the explanation

Explanation:

In this case, we have to keep in mind that in the monosubstituted product we only have to replace 1 hydrogen with another group. In this case, we are going to use the methyl group CH_3.

In the axial position, we have a more steric hindrance because we have two hydrogens near to the CH_3 group. If we have <u>more steric hindrance</u> the molecule would be <u>more unstable</u>. In the equatorial positions, we don't <u>any interactions</u> because the CH_3 group is pointing out. If we don't have <u>any steric hindrance</u> the molecule will be <u>more stable</u>, that's why the molecule will <u>the equatorial position.</u>

See figure 1

I hope it helps!

6 0
3 years ago
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