Answer:
This is the typical route of alcohol metabolism, where in the liver it is first transformed to acetaldehyde and then to acetate.
Explanation:
Ethanol is not digested but absorbed and follows its metabolic pathway in the liver, producing in the first instance acetaldehyde, which is the main substance that causes the hangover and then this compound is transformed into the final product, which is acetate Later acetate is metabolized to Acetyl-CoA. The enzyme responsible for the metabolism of ethanol is alcohol dehydrogenase in the liver, and for the cytochrome P-450 dependent system and for catalase in the liver.
Answer:
Please see the answer..hope its works
Explanation:
The NMR spectrometer will acquire data for the wrong chemical shift range and you will potentially have skewed data when opening spinworks-NMR spectrometer examines a specific 12 ppm range based on the expected solvent peak, and if a different solvent is used a different range may be examined
To explain further, If the user declares the wrong solvent, one of two things may happen. Firstly, the spectrometer may not be able to establish a deuterium lock and will report an error and not run the sample. Secondly, the spectrometer may be able to establish a lock despite the fact that the deuterium signal is off resonance. If the lock is established, the field strength will be set to a value appropriate to put the declared solvent signal on-resonance. When a proton NMR spectrum is collected, the chemical shift scale will be incorrect by an amount equal to the proton chemical shift difference between the true solvent and the declared solvent.
The total number of electron pairs that are shared between the two carbon atoms in a molecule of ethyne is 3.
1. D
2. A
3. B
4. C
5. E
6. I
7. J
8. L
9. M
10. G
11. H
12. K
13. F
