Hydrogen gas(H2) has a molar mass of 2 g. Molar mass of a substance is defined as the mass of 1 mole of that substance. And by 1 mole it is meant a collection of 6.022*10^23 particles of that substance.
So number of moles of H2 are 0.5 in this case. And thus it means there are (6.022*10^23)*0.5 particles( here they are molecules) in 1g of H2.
Explanation:
(A)role of nittogen fixing bacteria
=Nitrogen-fixing bacteria, microorganisms capable of transforming atmospheric nitrogen into fixed nitrogen (inorganic compounds usable by plants). More than 90 percent of all nitrogen fixation is effected by these organisms, which thus play an important role in the nitrogen cycle.
B)role of nitrifying bacteria
=Nitrifying bacteria convert the most reduced form of soil nitrogen, ammonia, into its most oxidized form, nitrate. In itself, this is important for soil ecosystem function, in controlling losses of soil nitrogen through leaching and denitrification of nitrate.
C)role of denitrifying bacteria
=Denitrifying bacteria converts nitrates back to nitrogen gas.
Always use least amount of sig figs possible. So this 9.7 would be (answer): 2 sig figs
Answer:
D. The electron-withdrawing fluorine atoms pull electron density from the oxygen in trifluoroacetate. The negative charge is more stabilized in trifluoroacetate by this effect.
Explanation:
The structures of trifluoroacetate and acetic acid are both shown in the image attached.
The trifluoroacetate anion (CF3CO2-), just like the acetate anion has in the middle, two oxygen atoms.
However, in the trifluoroacetate anion, there are also three electronegative fluorine atoms attached to the nearby carbon atom attached to the carbonyl, and these pull some electron density through the sigma bonding network away from the oxygen atoms, thereby spreading out the negative charge further. This effect, called the "inductive effect" stabilizes the anion formed,the trifouoroacetate anion is thus more stabilized than the acetate anion.
Hence, trifluoroacetic acid is a stronger acid than acetic acid, having a pKa of -0.18.
The enol carbon or ∝-carbon nucleophile attacks at molecular bromine in the acid-catalyzed α-bromination of a ketone
Treatment of ketones with bromine in the presence of acid will results in formation of a new C-Br bond at the alpha position. The purpose of the acid is to catalysed formation of the enol from ketone , which is active nucleophile in the reaction. This reaction is called haloform reaction which is used to identify the methyl substituted ketone in the presence of aldehyde.
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