Answer:
When secondary bile salts (or acids) lack a OH, they are reabsorbed
Explanation:
The lost of a hydroxyl group (OH) in the bile salts structure means less hydro solubility. Thus, they are not eliminated, conversely, the are reabsorbed for intestine and they go back to the liver.
I hope my answer helps
Answer:
4-oxopentanoic acid.
Explanation:
In this case, we must remember that the Grignard reaction is a reaction in which <u>carbanions</u> are produced. Carboanions have the ability to react with CO2 to generate a new C-C bond and a carboxylate ion. Finally, the acid medium will protonate the carboxylate to produce the <u>carboxylic acid group.
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The molecules that can follow the mechanism described above are the molecules: p-methylbenzoic acid, cyclopentane carboxylic acid and 3-methylbutanoic acid. (See figure 1)
In the case of <u>4-oxopentanoic acid</u>, the possible carbanion <u>will attack the carbonyl group</u> to generate a cyclic structure and an alcohol group (1-methylcyclopropan-1-ol). Therefore, this molecule cannot be produced by this reaction. (See figure 2)
I think the correct answer from the choices listed above is option A. A refracting telescope is made smaller than a reflecting telescope because small lenses cause less distortion in images than big lenses. <span> They are not subject to chromatic aberration because reflected light does not disperse according to wavelength.</span>
Do not ionize in solutions
Poor conductors of electricity/heat
Low melting/boiling points
gases or liquids at room temperature