Bronchodilators <span>are prophylactic agents used to treat bronchoconstriction.</span>
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.
Answer:
B
Explanation:
Heating a piece of iron until it glows.
Explanation:
Most reagent forms are going to absorb water from the air; they're called "hygroscopic". Water presence can have a drastic impact on the experiment being performed For fact, it increases the reagent's molecular weight, meaning that anything involving a very specific molarity (the amount of molecules in the final solution) will not function properly.
Heating will help to eliminate water, although some chemicals don't react well to heat, so it shouldn't be used for all. A dessicated environment is simply a means to "dry." That allows the reagent with little water in the air to attach with.
Polar liquids have both negative and positive ends.
