NaCl is salt to it is obviously SOLUBLE :)
Answer:
I believe the answer The case study was influenced by bias, and led to incorrect conclusions being drawn. plz correct me if I am wrong
Explanation:
Explanation:
Atomic radius decreases from left to right in a period.
Therefore Calcium would have a smaller atomic size.
Answer:
ionize
Explanation:
Acids are chemical substances that lose/donate their hydrogen ion (H+) when they react with water. This property of acids is termed IONIZATION. In a chemical reaction involving acids and bases, acids release their proton or hydrogen ion (H+) in the presence of water solutions to form a conjugate base, which is usually an anion.
For example, in the chemical reaction;
HX + H20 -------> X- + H30+
HX is the acid because it loses its electron to water and forms the anion, X-, which is the conjugate base. Hence, it can be said that acid HX ionizes in water.
Answer:
See explanation and picture below
Explanation:
First, in the case of methyloxirane (Also known as propilene oxide) the mechanism that is taking place there is something similar to a Sn2 mechanism. Although a Sn2 mechanism is a bimolecular substitution taking place in only step, the mechanism followed here is pretty similar after the first step.
In both cases, the H atom of the HBr goes to the oxygen in the molecule. You'll have a OH⁺ in both. However, in the case of methyloxirane the next step is a Sn2 mechanism step, the bromide ion will go to the less substitued carbon, because the methyl group is exerting a steric hindrance. Not a big one but it has a little effect there, that's why the bromide will rather go to the carbon with more hydrogens. and the final product is formed.
In the case of phenyloxirane, once the OH⁺ is formed, the next step is a Sn1 mechanism. In this case, the bond C - OH⁺ is opened on the side of the phenyl to stabilize the OH. This is because that carbon is more stable than the carbon with no phenyl. (A 3° carbon is more stable than a 2° carbon). Therefore, when this bond opens, the bromide will go there in the next step, and the final product is formed. See picture below for mechanism and products.