30.4 is the answer
<span> composition is: 58.8 0/0 C, 9.9 0/0 H, and 31.3 0/0 </span>O<span>. Ifit's molecular mass is 306 ... composition of the </span>compound<span> is </span>30.4<span>% </span>
Answer: sodium amide undergoes an acid -base reaction
Explanation:
sodium amide is a ionic compound and basically exists as sodium cation and amide anion. Amide anion is highly basic in nature and hence as soon as there is amide anion generated in the solution , Due to its very pronounced acidity it very quickly abstracts the slightly acidic proton available on methanol.
This leads to formation of ammonia and sodium methoxide.
Hence sodium amide reacts with methanol and abstracts its only acidic proton and form ammonia and sodium Methoxide.
Hence the 3rd statement is a corrects statement.
So we cannot use methanol for sodium amide because sodium amide itself would react with methanol and the inherent molecular natur of sodium amide would then change.
The 1st and 2nd statements both are incorrect because both the compounds methanol as well as sodium amide have dipole moments and hence are polar molecules.
The 4th statement is also incorrect as both the molecules have dipole moment and hence there would be ion-dipole forces operating between them.
The following reaction occurs:
NaNH₂+CH₃OH→NH₃+CH₃ONa
Answer:
Cows and other ruminant animals (like goats and sheep) emit methane, a potent greenhouse gas, as they digest grasses and plants. This process is called “enteric fermentation,” and it's the origin of cows' burps.
Explanation:
Hawaii, Iceland, and Yellowstone are examples of places that were formed by hot spot volcanoes.
Hope this helps!
During the transamination process, the enzyme transaminases use Pyridoxal pyrophosphate as a cofactor.
All transamination reactions, as well as several amino acid oxylation and deamination processes, involve the coenzyme pyridoxal phosphate. The aminotransferase enzyme's epsilon-amino group of a particular lysine group forms a Schiff-base bond with the aldehyde group of pyridoxal phosphate.
The epsilon-amino group of the lysine residue in the active site is replaced by the alpha-amino group of the amino acid substrate. The ensuing intermediate, a quinoid, undergoes deprotonation to become an aldimine, which is then protonated to become a ketimine by accepting a proton in a different position. Ketamine undergoes hydrolysis, leaving the amino group on the protein complex intact.
Know more about Pyridoxal pyrophosphate at:
brainly.com/question/14117818
#SPJ4
