Answer:
b) +2 and +3.
Explanation:
Hello,
In this case, given the molecular formulas:
And:
We can relate the subscripts with the oxidation states by knowing that they are crossed when the compound is formed, for that reason, we notice that oxygen oxidation state should be -2 for both cases and the oxidation state of X in the first formula must be +2 since both X and O has one as their subscript as they were simplified:
Moreover, for the second case the oxidation state of X should be +3 in order to obtain 3 as the subscript of oxygen:
Thus, answer is b)+2 and +3
Best regards.
Answer:
This question is incomplete
Explanation:
The question is incomplete because of the absence of the table but since the question says there are data from an investigation about a plant growth and five other plants (making six) of the same type, the best way to display this type of data for analyst is to use the grouped bar chart. <u>The grouped bar chart will display the data obtained (from an investigation on plant growth) from different students on each of the six plants (of the the same type)</u>.
Colours are usually used to identify the bars (of a group) or could be used to separate the group from other groups but in this case, colours are better used to identify the bars of a group.
Answer: After 4710 seconds, 1/8 of the compound will be left
Explanation:
Using the formulae
Nt/No = (1/2)^t/t1/2
Where
N= amount of the compound present at time t
No= amount of compound present at time t=0
t= time taken for N molecules of the compound to remain = 4710 seconds
t1/2 = half-life of compound = 1570 seconds
Plugging in the values, we have
Nt/No = (1/2)^(4710s/1570s)
Nt/No = (1/2)^3
Nt/No= 1/8
Therefore after 4710 seconds, 1/8 molecules of the compound will be left
The empirical formula is the simplest form of the formula expressed in the lowest ratio. In this case, we just have to divide each subscript by the greatest common factor. Hence.
a. CN
b. P2O5
c.N2O5
d.NaCl
e. C9H20
f. BH3
g.K2Cr2O7
h.AlB3
i.CH
j.SiCl4
Answer:
1,4-hexanediamine contains two 
functional groups.
Explanation:
1,4-hexanediamine is an organic molecule which contains two functional groups at C-1 and C-4 position.
The longest carbon chain in 1,4-hexanediamine contains six carbon atoms.
Molecular formula of 1,4-hexanediamine is 
.
1,4-hexanediamine used as a bidentate ligand in organometallic chemistry.
The structure of 1,4-hexanediamine is shown below.
