Answer:
The standard potential, E cell, for this galvanic cell is 0.5670V
Explanation:
Ni²⁺(aq) + 2e⁻ → Ni(s) E red = - 0.23V ANODE
Cu²⁺(aq) + 2e- → Cu(s) E red = + 0.337V CATHODE
ΔE° = E cathode - E anode
ΔE° = 0.337V - (0.23V) = 0.5670 V
Answer is: <span>concentration of NOCl is 3.52 M.
</span>
Balanced chemical reaction: 2NOCl(g) ⇄ 2NO(g) + Cl₂<span>(g).
Kc = 8.0.
</span>[NOCl] = 1.00 M; equilibrium concentration.
[NO] = x.
[Cl₂] = x/2; equilibrium concentration of chlorine.<span>
Kc = </span>[Cl₂] ·[NO]² / [NOCl].
8.00 = x/2 · x² / 1.
x³/2 = 8.
x = ∛16.
x = 2.52 M.
co(NOCl) = [NOCl] + x.
co(NOCl) = 1.00 M + 2.52 M.
co(NOCl) = 3.52 M; the initial concentration of NOCl.
Explanation:
A strip of solid palladium metal is put into a beaker of nicl2
Palladium (Pd) + Nickel Chloride (NiCl2)
To answer this question properly you must refer to the reactivity series.
The activity series is a chart of metals listed in order of declining relative reactivity. The top metals are more reactive than the metals on the bottom.
In this series, Nickel is higher than Palladium. This means that if a Palladium strip is placed into a solution of a Ni salt, then a reaction will not take place, nothing would happen.
Because Pd is lower than Ni in the reactivity series.
There is no reaction so no equation.
Answer:
a, g, c
Explanation:
The conversion of the stable cyclopentane into Trans-1, 2dibromocyclopentane will require three step reactions.
The first is to convert the compound into a cyclopentene, through the addition of Bromine water under heat and photons (light). So option A is the first in the order. This will generate 1 bromocyclopentane through halogenation of the alkane. Secondly, a hot and strong base should be added like the NaOEt, EtOH to remove the added bromine and one atom of hydrogen from the resulting 1 bromocyclopentane in the previous reaction. This will yield cyclopentene, thus making the compound more electrophilic. So option g is required. Thirdly, bromine molecules will be added (C) to take up their places at the two electrophilic regions of the compound to produce Trans-1, 2dibromocyclopentane.
