It is alkaline ........I need 20 characters......
Answer:
pH = 10.38
Explanation:
∴ molar mass C9H13N = 135.21 g/mol
∴ pKb = - log Kb = 4.2
⇒ Kb = 6.309 E-5 = [OH-][C9H20O3N+] / [C9H13N]
∴ <em>C</em> sln = (205 mg/L )*(g/1000 mg)*(mol/135.21 g) = 1.516 E-3 M
mass balance:
⇒ <em>C</em> sln = 1.516 E-3 = [C9H20O3N+] + [C9H13N]......(1)
charge balance:
⇒ [C9H20O3N+] + [H3O+] = [OH-]; [H3O+] is neglected, come from water
⇒ [C9H20O3N+] = [OH-].......(2)
(2) in (1):
⇒ [C9H13N] = 1.516 E-3 - [OH-]
replacing in Kb:
⇒ Kb = 6.3096 E-5 = [OH-]² / (1.516 E-3 - [OH-])
⇒ [OH-]² + 6.3096 E-5[OH] - 7.26613 E-8 = 0
⇒ [OH-] = 2.3985 E-4 M
∴ pOH = - Log [OH-]
⇒ pOH = 3.62
⇒ pH = 14 - pOH = 14 - 3.62 = 10.38
Answer:
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Explanation:
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What u have to tell us what to do
Answer:
See explanation
Explanation:
In a chemical reaction, a particular reaction path may be favoured due to the fact that it is energetically more favourable(lower energy sigma complex is formed).
The more the resonance structures produced in a particular reaction pathway, the more energetically favourable it is.
In the chlorination of bromobenzene, ortho attack and para attack are preferred because each of these pathways involves a sigma complex with__4________resonance structures. Attack at the meta position involves formation of a sigma complex with only____3_______ resonance structures. The reaction will proceed more rapidly via the_____lower_______ energy sigma complex, so attack takes place at the ortho and para positions in preference to the meta position.