Answer: Option (c) is the correct answer.
Explanation:
When an acid or base is added to a solution then any resistance by the solution in changing the pH of the solution is known as a buffer.
This is because a buffer has the ability to not get affected by the addition of small amounts of an acid or a base. As a result, it helps in maintaining the pH of the solution.
In the give case, when we add the HCl then more number of protons will dissociate. This causes the acetate to react with the protons and leads to the formation of acetic acid.
We know that acetic acid is a weak acid and it dissociates partially or feebly. Therefore, no change in pH will take place.
Thus, we can conclude that equation
represents the chemical reaction that accounts for the fact that acid was added but there was no detectable change in pH.
Answer: There are 0.000043 moles of melatonin.
Explanation:
According to avogadro's law, 1 mole of every substance occupies 22.4 L at STP and contains avogadro's number
of particles.
To calculate the moles, we use the equation:

given mass = 10 mg = 0.01 g
molar mass of
= 232.28 g
Thus there are 0.000043 moles of melatonin
The best answer for the question above would be the chloroflourocarbons or the CFCs. These chloroflourocarbons or CFCs are the ones responsible for the depletion of the ozone - which leads to leaving a hole in its layer. These gases eat out the ozone layer and allows harmful UV rays of the sun to come in the Earth.
Answer:
aldehyde
carbon-1
ketone
carbon-2
Explanation:
Monosaccharides are colorless crystalline solids that are very soluble in water. Moat have a swwet taste. D-Fructose is the sweetest monosaccharide.
In the open chain form, monosaaccharides have a carbonuyl group in one of their chains. If the carbonyl group is in the form of an aldehyde group, the monosaccharide is an aldose; if the carbonyl group is in the form of a ketone group, the monosaccharide is known as a ketose. glucose is an aldose while fructose is a ketose.
In D-glucose, there is an aldehyde functional group, and the carbonyl group is at carbon-1 when looking at the Fischer projection.
In D-fructose, there is a ketone functional group, and the carbonyl group is at carbon-2 when looking at the Fischer projection.