D. Electrons
Atoms can share their electrons in order to create bonds with other atoms
Just use the Heisenberg Uncertainty principle:
<span>ΔpΔx = h/2*pi </span>
<span>Δp = the uncertainty in momentum </span>
<span>Δx = the uncertainty in position </span>
<span>h = 6.626e-34 J s (plank's constant) </span>
<span>Hint: </span>
<span>to calculate Δp use the fact that the uncertainty in the momentum is 1% (0.01) so that </span>
<span>Δp = mv*(0.01) </span>
<span>m = mass of electron </span>
<span>v = velocity of electron </span>
<span>Solve for Δx </span>
<span>Δx = h/(2*pi*Δp) </span>
<span>And that is the uncertainty in position. </span>
Answer:
The order of reactivity towards electrophilic susbtitution is shown below:
a. anisole > ethylbenzene>benzene>chlorobenzene>nitrobenzene
b. p-cresol>p-xylene>toluene>benzene
c.Phenol>propylbenzene>benzene>benzoic acid
d.p-chloromethylbenzene>p-methylnitrobenzene> 2-chloro-1-methyl-4-nitrobenzene> 1-methyl-2,4-dinitrobenzene
Explanation:
Electron donating groups favor the electrophilic substitution reactions at ortho and para positions of the benzene ring.
For example: -OH, -OCH3, -NH2, Alkyl groups favor electrophilic aromatic substitution in benzene.
The -I (negative inductive effect) groups, electron-withdrawing groups deactivate the benzene ring towards electrophilic aromatic substitution.
Examples: -NO2, -SO3H, halide groups, Carboxylic acid groups, carbonyl gropus.
Answer:
A (True)
Explanation:
Because ibuprofen has a chiral carbon center (carbon bonded to 4 distinct groups of atoms).
This means that a mixture of ibuprofen can rotate plane-polarized light equally in both the clockwise and counterclockwise direction.
Answer:
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Explanation: