Answer:
2Ag⁺ (aq) + CrO₄⁻² (aq) ⇄ Ag₂CrO₄ (s) ↓
Ksp = [2s]² . [s] → 4s³
Explanation:
Ag₂CrO₄ → 2Ag⁺ + CrO₄⁻²
Chromate silver is a ionic salt that can be dissociated. When we have a mixture of both ions, we can produce the salt which is a precipitated.
2Ag⁺ (aq) + CrO₄⁻² (aq) ⇄ Ag₂CrO₄ (s) ↓ Ksp
That's the expression for the precipitation equilibrium.
To determine the solubility product expression, we work with the Ksp
Ag₂CrO₄ (s) ⇄ 2Ag⁺ (aq) + CrO₄⁻² (aq) Ksp
2 s s
Look the stoichiometry is 1:2, between the salt and the silver.
Ksp = [2s]² . [s] → 4s³
Answer:The first task of a nuclear weapon design is to rapidly assemble a supercritical mass of fissile uranium or plutonium. A supercritical mass is one in which the percentage of fission-produced neutrons captured by another fissile nucleus is large enough that each fission event, on average, causes more than one additional fission event. Once the critical mass is assembled, at maximum density, a burst of neutrons is supplied to start as many chain reactions as possible. Early weapons used a modulated neutron generator codenamed "Urchin" inside the pit containing polonium-210 and beryllium separated by a thin barrier. Implosion of the pit crushed the neutron generator, mixing the two metals, thereby allowing alpha particles from the polonium to interact with beryllium to produce free neutrons. In modern weapons, the neutron generator is a high-voltage vacuum tube containing a particle accelerator which bombards a deuterium/tritium-metal hydride target with deuterium and tritium ions. The resulting small-scale fusion produces neutrons at a protected location outside the physics package, from which they penetrate the pit. This method allows better control of the timing of chain reaction initiation.
Explanation:
Answer:
I can't draw but you could draw 2 electrons in the first orbit and 3 electrons in the second orbit.
Explanation:
Answer:
IV
Explanation:
The complete question is shown in the image attached.
Let us call to mind the fact that the SN1 mechanism involves the formation of carbocation in the rate determining step. The order of stability of cabocations is; tertiary > secondary > primary > methyl.
Hence, a tertiary alkyl halide is more likely to undergo nucleophilic substitution reaction by SN1 mechanism since it forms a more stable cabocation in the rate determining step.
Structure IV is a tertiary alkyl halide, hence it is more likely to undergo nucleophilic substitution reaction by SN1 mechanism.