Answer:
Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Explanation:
The benzene ring in itself does not easily undergo electrophilic substitution reaction. Some groups activate or deactivate the benzene ring towards electrophilic substitution reactions.
-NO2 ia a highly deactivating substituent therefore, Friedel-Crafts alkylation of nitrobenzene does not take place under any conditions.
This reaction scheme is therefore flawed because Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Your correct answer is (B) Ratio of neutrons to protons
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Answer:
because the tectonic plates move 4 inches per year.
Explanation:
Answer:
A mixture of 100. mL of 0.1 M HC3H5O3 and 50. mL of NaOH
Explanation:
The pH of a buffer solution is calculated using following relation

Thus the pH of buffer solution will be near to the pKa of the acid used in making the buffer solution.
The pKa value of HC₃H₅O₃ acid is more closer to required pH = 4 than CH₃NH₃⁺ acid.
pKa = -log [Ka]
For HC₃H₅O₃
pKa = 3.1
For CH₃NH₃⁺
pKa = 10.64
pKb = 14-10.64 = 3.36 [Thus the pKb of this acid is also near to required pH value)
A mixture of 100. mL of 0.1 M HC3H5O3 and 50. mL of NaOH
Half of the acid will get neutralized by the given base and thus will result in equal concentration of both the weak acid and the salt making the pH just equal to the pKa value.
Answer: the system of blood, blood vessels and the heart that carries blood throughout the body
Explanation: i hope this helps