A) LITHIUM is the least reactive alkali metal
B) FRANCIUM is the most reactive alkali metal
C) BERYLLIUM is the least reactive alkaline earth metal
D) RADIUM is the most reactive alkaline earth metal
E) TENNESSINE is the most reactive halogen
For E it might also be Astatine because Tennessine is a fairly new
Answer:
It changes as they grow
Or when they start to have an unhealthy diet
Answer:
C.
Explanation:
The electronic configuration of N (7 electrons): 1s² 2s² 2p³.
The orbital 1s is filled with two electrons and their spinning direction is opposite and also electrons of 2s.
3p contains (3 electrons) should fill the 3 orbitals firstly. Every orbital contains 1 electron and be in the same spin direction.
So, the right choice is c.
A is wrong because 2 electrons of 3p are paired in the first orbital before filling every orbital.
B is wrong because the 2 electrons of 1s and 2s are in the same direction and also 2 electrons of 3p are paired in the first orbital before filling every orbital.
D is also wrong the 2 electrons of 1s and 2s are in the same direction and the electron in the second orbital of 3p are in opposite direction of the other 2 electrons.
Answer:
a chemical substance that neutralizes alkalis, dissolves some metals, and turns litmus red; typically, a corrosive or sour-tasting liquid of this kind.
Explanation:
Answer:
The structure with the ring flipped is the most stable
Explanation:
We have the trans 1,2 - dimethylcyclohexane. With the wedge/dash structure we could not figure is this form is stable (If we do a comparison with the cis structure). But when we do a chair structure and ring flipped structure, this is easier to look.
The picture attached shows the structures, they are labeled as 1, 2 and 3, according to this problem.
In the chair structure, according to the picture below, you can see that both methyls are heading in the axial positions of the ring (One facing upward and the other downward). This is pretty stable, however, when the methyls are in those positions, the methyl position 1, can undergoes an 1,3 diaxial interactions with the hydrogens atoms (They are not drawn, but still are there), so this interaction makes this structure a little less stable that it can be.
On the other side, the ring flipped structure, we can see that both methyls are in the equatorials positions of the ring, and in these positions, it can avoid the 1,4 diaxial interactions with the hydrogens atoms, making this structure the most stable structure.
Hope this helps
