The answer is B. Enzymes.
Enzymes are biological catalysts that help cause reactions in your body.
<span>the pH of a 0.050 M triethylamine, is 11.70
</span>
For triehtylamine,
, the reaction will be
and we know, pH = -log[H+] and pOH = -log[OH-]
Also, pOH + pH = 14
Now, the Kb value = 5.3 x 10^-4
And
![kb = \frac{( [( C_{2}H_{5})_{3}NH^{+} ]* OH^{-} )}{[( C_{2}H_{5})_{3}N]}](https://tex.z-dn.net/?f=kb%20%3D%20%20%5Cfrac%7B%28%20%5B%28%20C_%7B2%7DH_%7B5%7D%29_%7B3%7DNH%5E%7B%2B%7D%20%5D%2A%20%20OH%5E%7B-%7D%20%29%7D%7B%5B%28%20C_%7B2%7DH_%7B5%7D%29_%7B3%7DN%5D%7D%20)
thus, [OH-] =(5.3 ^ 10-4) ^2 / 0.050
=0.00516 M
Thus, pOH = 2.30
pH = 14 - pOH = 11.7
Answer:
See explanation
Explanation:
A. Constitutional or structural isomers have the same molecular formula but different structural formulas.
B. Conformational isomers are compounds having the same atom to atom connectivity but differ by rotation about one or more single bonds.
C. Stereo isomers are compounds having the same molecular mass and atom to atom connectivity but different arrangement of atoms and groups in space.
I. Enantiomers are stereo isomers (optical isomers particularly) that are non-superimposable mirror images of each other.
II. Diasteromers are optical isomers that are not mirror images of each other.
Both diasteromers and enantiomers are types of optical isomers which in turn is one of the types of stereo isomers.
Stereo isomers differ from conformational isomers in that the arrangement of atoms in stereo isomers is permanent while conformational isomers results from free rotations in molecules about single bonds.
