Answer:
Explanation:
Catalysts lower activation energy. TRUE.
They provide an alternate pathway with a lower activation energy.
Catalysts are consumed by the overall reaction. FALSE.
They take part in the reaction, but they can be recovered unchanged at the end.
Catalysts speed up the chemical reactions. TRUE.
If the activation energy is lowered, a greater percentage of the molecules will have enough energy to get over the energy barrier.
Its like lowering the high-bar in a track and field meet. The lower the bar, the more athletes will be able to get over it.
Answer:
B) CH3(CH2)10CO2H
Explanation:
Hello,
In this case, we define amphipathic as a compound having both a hydrophilic and a hydrophobic part, for that reason, the hydrophilic part will be water-soluble (polar) whereas the hydrophobic does not (nonpolar). In such a way, some functional groups such as hydroxyl and carboxyl tend to be polar by cause of the presence of O-H bonds whereas long-carboned chains tend to be nonpolar by cause of the presence of C-H and C-C bonds.
Therefore, since A) CH3CH2OH (ethanol) and D) CH3CO2H (acetic acid) are short-carboned chains with polar groups they are largely hydrophilic whereas C) CH3(CH2)10CH3 (dodecane) is highly nonpolar, we sum up that only B) CH3(CH2)10CO2H (dodecanoic acid or lauric acid) is amphoteric as it has a long-charboned part (nonpolar) and a water-soluble part (polar).
Best regards.
Answer:
(edit: nvm I figured it out, here is the answer)
Explanation:
The small intestine i think :) hope that helps
Answer:
c and d, are you supposed to check 3? or only 2?