<u>Answer:</u> The limiting reagent in the reaction is bromine.
<u>Explanation:</u>
Limiting reagent is defined as the reagent which is completely consumed in the reaction and limits the formation of the product.
Excess reagent is defined as the reagent which is left behind after the completion of the reaction.
Given values:
Moles of iron = 10.0 moles
Moles of bromine = 12.0 moles
The chemical equation for the reaction of iron and bromine follows:

By the stoichiometry of the reaction:
If 3 moles of bromine reacts with 2 moles of iron
So, 12.0 moles of bromine will react with =
of iron
As the given amount of iron is more than the required amount. Thus, it is present in excess and is considered as an excess reagent.
Hence, bromine is considered a limiting reagent because it limits the formation of the product.
Thus, the limiting reagent in the reaction is bromine.
Answer:
K loses one electron to CI
Explanation:
The lewis electron dot notation shows only the chemical symbol of the element surrounded by dots to represent the valence electrons.
We have atom of K with one valence electrons
Cl with 7 valence electrons
For an electrostatic attraction to occur, both particles must be charged. To do this, one of the species must lose an electron, and the other gains it.
This will make both species attain a stable octet;
Hence, K will lose 1 electron and Cl will gain the electrons.
B
mass of solute - 4.0 g
mass of solution - 100g + 4.0g = 104g
4/104 = 0.03846
0.03846 • 100 = 3.8%
Answer:
Axial
Explanation:
In the most stable conformation of Cis-3-tert-Butylcyclohexanol, the tert-butyl group is at equatorial position and the alcohol group is in the axial position.
If the tert-butyl group is placed in equatorial position, repulsions are minimized. The bulkier the group, the greater the energy difference between the axial and equatorial conformers. Hence for a ring having a bulky substituent, such bulky substituent is better placed in the equatorial position.
The energy difference between the conformers of Cis-3-tert-Butylcyclohexanol is so high that the compound is almost "frozen" in a conformation where the tert-butyl groups are equatorial and the -OH groups are axial. This conformer is more stable by 24 KJ/mol.