Answer:
A. False.
Every substance contains the same number of molecules i.e 6.02x10^23 molecules
B. False.
Mass conc. = number mole x molar Mass
Mass conc. of 1mole of N2 = 1 x 28 = 28g
Mass conc. of 1mol of Ar = 1 x 40 = 40g
The mass of 1mole of Ar is greater than the mass of 1mole of N2
C. False.
Molar Mass of N2 = 2x14 = 28g/mol
Molar Mass of Ar = 40g/mol
The molar mass of Ar is greater than that of N2.
Explanation:
Photosynthesis takes carbon dioxide, water and sunshine and turn them into glucose and oxygen
Explanation
Glucose is the principal carbohydrate formed through photosynthesis, Through the process of photosynthesis sunshine, carbon dioxide and water to form glucose and oxygen
Equation for reaction is as follows
CO2+ H2O + light energy → C6H12O6 +O2
C6H12O6 is the glucose
Answer:
C. Lithium
Explanation:
This image describes the trend in reactivity. Group 1 metals are always the most reactive so yeah :)
Answer:
Basically, paramagnetic and diamagnetic refer to the way a chemical species interacts with a magnetic field. More specifically, it refers to whether or not a chemical species has any unpaired electrons or not.
A diamagnetic species has no unpaired electrons, while a paramagnetic species has one or more unpaired electrons.
Now, I won't go into too much detail about crystal field theory in general, since I assume that you're familiar with it.
So, you're dealing with the hexafluorocobaltate(III) ion, [CoF6]3â’, and the hexacyanocobaltate(III) ion, [Co(CN)6]3â’.
You know that [CoF6]3â’ is paramagnetic and that [Co(CN)6]3â’ is diamagnetic, which means that you're going to have to determine why the former ion has unpaired electrons and the latter does not.
Both complex ions contain the cobalt(III) cation, Co3+, which has the following electron configuration
Co3+:1s22s22p63s23p63d6
For an isolated cobalt(III) cation, all these five 3d-orbitals are degenerate. The thing to remember now is that the position of the ligand on the spectrochemical series will determine how these d-orbtals will split.
More specifically, you can say that
a strong field ligand will produce a more significant splitting energy, Δ a weak field ligand will produce a less significant splitting energy, Δ
Now, the spectrochemical series looks like this
http://chemedu.pu.edu.tw/genchem/delement/9.htmhttp://chemedu.pu.edu.tw/genchem/delement/9.htm
Notice that the cyanide ion, CNâ’, is higher on the spectrochemical series than the fluoride ion, Fâ’. This means that the cyanide ion ligands will cause a more significant energy gap between the eg and t2g orbitals when compared with the fluoride ion ligands.
http://wps.prenhall.com/wps/media/objects/3313/3393071/blb2405.htmlhttp://wps.prenhall.com/wps/media...
In the case of the hexafluorocobaltate(III) ion, the splitting energy is smaller than the electron pairing energy, and so it is energetically favorable to promote two electrons from the t2g orbitals to the eg orbitals → a high spin complex will be formed.
This will ensure that the hexafluorocobaltate(III) ion will have unpaired electrons, and thus be paramagnetic.
On the other hand, in the case of the hexacyanocobaltate(III) ion, the splitting energy is higher than the electron pairing energy, and so it is energetically favorable to pair up those four electrons in the t2g orbitals → a low spin complex is formed.
Since it has no unpaired electrons, the hexacyanocobaltate(III) ion will be diamagnetic.
It will slowly rotten and turn brown
