Answer:
Properties: The melting point of phosphorus (white) is 44.1°C, boiling point (white) is 280°C, specific gravity (white) is 1.82, (red) 2.20, (black) 2.25-2.69, with a valence of 3 or 5. There are four allotropic forms of phosphorus: two forms of white (or yellow), red, and black (or violet).Oct 7, 2019
Atomic Number: 15
Atomic Weight: 30.973762
Explanation:
: )
Answer:
HCl(aq) + KOH(aq) ⇒ KCl(aq) + H₂O(l)
Explanation:
Hydrochloric acid is an acid because it releases H⁺ in an aqueous solution.
Potassium hydroxide is a base because it releases OH⁻ in an aqueous solution.
When an acid reacts with a base they form a salt and water. This is a neutralization reaction. The neutralization reaction between hydrochloric acid and potassium hydroxide is:
HCl(aq) + KOH(aq) ⇒ KCl(aq) + H₂O(l)
The standard state of the elements Nitrogen and Oxygen are N2 and O2, knowing that they are diatomic elements. With that piece of information, the unbalanced equation for the formulation of NO2(g) should be as follows -
N2 + O2 ---> NO2
And if you include their states -
N2 ( g ) + O2 ( g ) ---> NO2 ( g )
To balance this chemical equation consider the number of reactants and products on other side of the equation. If you were to include a coefficient of one - half with respect to N2 on the reactant side, it would balance the reactants and products -
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.
Picometre is equal to 1·10⁻¹²m
175·10⁻¹² m = 1,75·10⁻¹⁰ m