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Leni [432]
3 years ago
8

Which statement is true about the atoms in helium gas?

Chemistry
1 answer:
jasenka [17]3 years ago
5 0

Answer: The answer is they are not closely packed

Explanation: HOPE THIS HELPS!!

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Identify the reactants and products in the following chemical equation: Zn +2HCl --> ZnCl2 + H2 *
Ad libitum [116K]

Answer:

A.

Explanation:

zinc and hydrochloric acid reacts to form zinc chloride and hydrogen.

hope it helps. :)

7 0
3 years ago
What do an electron and a neutron have in common?
zmey [24]
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). 
4 0
3 years ago
Read 2 more answers
What effect does adding a neutron have on the atoms identity
Sergeu [11.5K]

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.

5 0
3 years ago
Potassium hydroxide is classified as an arrhenius base because koh contains
mixas84 [53]

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.

KOH\rightarrow K^++OH^-

8 0
3 years ago
When methyloxirane is treated with HBr, the bromide ion attacks the less substituted position. However, when phenyloxirane is tr
konstantin123 [22]

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.

4 0
3 years ago
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