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08 is an integer and so fraction form in the simplest form is 8/1.08 is an integer and so fraction form in the simplest form is 8/1.08 is an integer and so fraction form in the simplest form is 8/1.08 is an integer and so fraction form in the simplest form is 8/1.
Child is the full form of child.
simplest form, reduced form, free form
plz advice me whether Form m & Form c.16 is same or not?
The plural form is digits; the singular form is digit.
The pKa value of a compound when it is protonated refers to the pH at which half of the compound is in its protonated form and half is in its deprotonated form.
The formula for the protonated form of H2O, which is when a hydrogen ion (H+) is added to water, is H3O+. This ion is also known as the hydronium ion.
The pKa value of protonated pyrrole is approximately 0.8.
At pH 1, serine is predominantly in its protonated form with a positively charged amino group (NH3+) and a deprotonated carboxyl group (COO-). This gives serine an overall positive charge.
Yes, if the pH is less than the pKa, the compound will be protonated.
A protonated water molecule is also known as a hydronium ion (H3O+).
Methyl indicator is typically found in its protonated form, which means it has the potential to act as a weak base when it accepts a proton.
When sodium phenoxide is reacted with CO2 and HCl, the phenoxide anion is protonated by HCl to form phenol. The phenol then reacts with CO2 to form salicylic acid.
When pyridine reacts with sodamide, the products obtained are sodamide anion (NaNH2) and a protonated pyridine molecule. The NaNH2 acts as a strong base and abstracts a proton from the pyridine molecule to form sodamide anion and a protonated pyridine.
If pH increases, then the solution is less protonated. The pH of a solution is defined as -log[H+], so when the concentration of hydrogen ions increases, the pH decreases.
In acidic medium, the hydroxyl group of the tertiary alcohol can be protonated, making it easier to lose a proton and form a carbocation intermediate, which is more stable due to hyperconjugation. This facilitates the oxidation process compared to in neutral or alkaline medium where the hydroxyl group is not protonated and the carbocation intermediate is less stable.
The pKa of CH3NH2, also known as methylamine, is approximately 10.7. This means that at a pH lower than 10.7, methylamine will predominantly exist in its protonated form, while at a pH higher than 10.7, it will exist primarily in its deprotonated form.