You can differentiate between ionic, covalent and molecular compounds by the fact that ionic compounds contain elements that include both a metal and a nonmetal. Molecular compounds contain both non metals covalently bonded to each other. While acids most often on their chemical formula start with the element of Hydrogen - H.
For Eg - sulphuric acid
H2SO4
hydrochloric acid - HCl.
Many of the actual chemicals in flower petals that give them their different colors are called anthocyanins. These are water-soluble compounds that belong to a bigger class of chemicals known as flavonoids. Anthocyanins are responsible for creating the colors blue, red, pink, and purple in flowers.
Before proceeding, we should write the reaction equation to better understand what is happening:
2AgNO₃ + Na₂S → Ag₂S + 2NaNO₃
Now, we may apply the law of conservation of mass, due to which the total mass before a chemical reaction is equivalent to the total mass after a chemical reaction. Therefore:
Mass of silver nitrate + mass of sodium sulfide = mass of silver sulfide + mass of sodium nitrate
Mass of silver nitrate + 156.2 = 595.8 + 340
Mass of silver nitrate = 779.6 grams
I believe the most appropriate answer would be to change the core from wood to iron. This is because iron is a magnetic material while wood is not magnetic hence cant acquire magnetism. Other factors that would increase the strength of electromagnet would be; increasing the amount of electric current, and increasing the number of windings.
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.