Answer:
A.
Explanation:
zinc and hydrochloric acid reacts to form zinc chloride and hydrogen.
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What an electron and a neutron have in common is that <u>each particle exists inside an atom,</u>
Atoms consist of three particles: protons (which are positively charged), electrons (which are negatively charged), and neutrons (which have no charge).
Neutrons don’t carry an electrical charge, meaning that adding or subtracting them from the nucleus will not change the electrical charge of the nucleus of an atom. But, adding/removing neutrons changes the mass of the nucleus. This is how isotopes are formed.
Answer: hydroxide ions
Explanation:
According to the Arrhenius concept, an acid is a substance that ionizes in the water to give hydronium ion or hydrogen ion and a bases is a substance that ionizes in the water to give hydroxide ion .
According to the Bronsted Lowry conjugate acid-base theory, an acid is defined as a substance which donates protons and a base is defined as a substance which accepts protons.
According to the Lewis concept, an acid is defined as a substance that accepts electron pairs and base is defined as a substance which donates electron pairs.
As KOH can give hydroxide ions on dissociation , it is considered as arrhenius base.

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.