Answer:
Kinetic energy
Explanation:
This is the energy possessed by a moving object.
Answer : The percentage reduction in intensity is 79.80 %
Explanation :
Using Beer-Lambert's law :



where,
A = absorbance of solution
C = concentration of solution = 
l = path length = 2.5 mm = 0.25 cm
= incident light
= transmitted light
= molar absorptivity coefficient = 
Now put all the given values in the above formula, we get:



If we consider
= 100
then, 
Here 'I' intensity of transmitted light = 20.198
Thus, the intensity of absorbed light
= 100 - 20.198 = 79.80
Now we have to calculate the percentage reduction in intensity.


Therefore, the percentage reduction in intensity is 79.80 %
Answer:
Judging from the wording of he question, you mean units. If that is indeed the case, the answer is g/Mol (grams per mol)
Let me know if my interpretation is incorrect and please tell me what you are actually trying to find.
The question is incomplete. Complete question is attached below
..............................................................................................................................
Correct Answer:
Option C i.e. I ~ III < IV < V < II
Reason:
During a nucleophilic subsitution reaction of chloroarenes, Cl- group is replaced by an nucleophile like OH-.
Order of reactivity, during such reactions depends on the electron density on carbon atom that is attached to Cl. Lower the electron density, greater will be the reactivity.Among the provided chloroarenes, electron density on C atom will be minimum in case of compound II, because of presence of electron withdrawing group (-NO2) at ortho and para position. Due to this, there will be large number of resonating structures. This signifies greater electron de-localization, and hence largest reactivity for nucleophilic substitution reaction.
Followed by this, compound V will show greater reactivity, due to presence of -NO2 group at para and one of the ortho position. Compound IV will have less number of resonating structures as compared to compound II and V, hence it will display poor reactivity towards nucleophilic substitution reaction.
Finally, compound 1 and III will minimum reactivity towards nucleophilic substitution reaction, because -NO2 group present at meta position (compound III) will not participate in resonance.
Answer:
2,2,3,3-tetrapropyloxirane
Explanation:
In this case, we have to know first the alkene that will react with the peroxyacid. So:
<u>What do we know about the unknown alkene? </u>
We know the product of the ozonolysis reaction (see figure 1). This reaction is an <u>oxidative rupture reaction</u>. Therefore, the double bond will be broken and we have to replace the carbons on each side of the double bond by oxygens. If
is the only product we will have a symmetric molecule in this case 4,5-dipropyloct-4-ene.
<u>What is the product with the peroxyacid?</u>
This compound in the presence of alkenes will produce <u>peroxides.</u> Therefore we have to put a peroxide group in the carbons where the double bond was placed. So, we will have as product <u>2,2,3,3-tetrapropyloxirane.</u> (see figure 2)