Well its Organic Chemistry... and is the Fractional Distillation of Crude Oil
Answer:
pH = 1.33
Explanation:
Because HCl is a strong acid, each mole of HCl will completely dissociate into H⁺ and Cl⁻ species.
Now we calculate the molar concentration (molarity) of H⁺:
- Molarity = moles / volume
(750 mL ⇒ 750 / 1000 = 0.750 L)
- Molarity = 0.035 moles / 0.750 L
Then we calculate the pH of the solution:
Answer:
Gold is a metal, more specifically a transition metal, whereas Oxygen is a nonmetal, more specifically a reactive nonmetal. Using this information, you can compare and contrast metals, nonmetals, and metalloids.
Metals are:
Shiny
High melting point
Mostly silver or gray in color
Mostly solids at room temperature – Mercury (Hg) is a liquid at room temperature
Malleable – able to be hammered into a thin sheet
Ductile – able to be drawn/pulled into a wire
Good conductors of heat and electricity
Nonmetals are:
Dull
Low melting point
Brittle – break easily
Not malleable
Not ductile
Poor conductors of heat and electricity
Metalloids are:
Found on the “zig-zag” line on the Periodic Table of Elements
Have properties of both metals and nonmetals
Can be shiny or dull
Semiconductors – able to conduct electricity under certain conditions
Explanation:
Reccomend this site for questions llike these: https://ptable.com/#Properties
Answer:
Mostly Para
Explanation:
First, let's assume that the molecule is the toluene (A benzene with a methyl group as radical).
Now the nitration reaction is a reaction in which the nitric acid in presence of sulfuric acid, react with the benzene molecule, to introduce the nitro group into the molecule. The nitro group is a relative strong deactiviting group and is metha director, so, further reactions that occur will be in the metha position.
Now, in this case, the methyl group is a weak activating group in the molecule of benzene, and is always ortho and para director for the simple fact that this molecule (The methyl group) is a donor of electrons instead of atracting group of electrons. Therefore for these two reasons, when the nitration occurs,it will go to the ortho or para position.
Now which position will prefer to go? it's true it can go either ortho or para, however, let's use the steric hindrance principle. Although the methyl group it's not a very voluminous and big molecule, it still exerts a little steric hindrance, and the nitro group would rather go to a position where no molecule is present so it can attach easily. It's like you have two doors that lead to the same place, but in one door you have a kid in the middle and the other door is free to go, you'll rather pass by the door which is free instead of the door with the kid in the middle even though you can pass for that door too. Same thing happens here. Therefore the correct option will be mostly para.
I think the answer is a i hope it helps
