Answer:
Here's what I find.
Explanation:
a. Structure
Acebutolol is a secondary amine (basic). It forms a substituted ammonium salt when treated with hydrochloric acid.
The structure of the salt is shown below, with a red arrow pointing toward the positive charge on the N atom.
b. Solubility
The formula of acebutolol is C₁₈H₂₈N₂O₄.
The amide, acetyl, and ether groups confer little solubility to the molecule.
The alcohol and secondary amine do confer some solubility, because they can donate and accept hydrogen bonds.
However, they can each overcome the hydrophobic properties of only three to five carbons, and acebutolol has 18 of them.
The free amine would be preferentially soluble in lipid material (fats)
The protonated amine is ionic and therefore much more soluble in aqueous media (e.g., blood).
c. Marketing
The drug must be delivered to the tissues of the heart, where it blocks the effects of adrenalin. The best way to do this is through the blood, so acebutolol is marketed as the hydrochloride salt.
Yes (Al) Aluminum and (S) Sulfur would make an ionic compound because you need a metal and a nonmetal to make an ionic compound.
Answer:
D.
Explanation:
Hello!
In this case, for the given set of chemical reactions, it is possible to infer that D. is a categorized as redox due to the following:
Since both chlorine and bromine remain as diatomic gases, their oxidation states in such a form is 0, but as anions with lithium cations they have a charge of - according to the following reaction and half-reactions:
Unlike the other reactions whereas no change in the oxidation states is evidenced.
I think its A sorry if im wrong
Answer:The changes around us that involves chemistry is burning,cooking,rusting,and rotting.
Explanation: