Elements in the same period Question 7 options: A) form bonds with the same type of elements. B) have the same number of protons
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The pink color in the solution fades. Some of the colored indicator ion converts to the colorless indicator molecule.
<h3>Explanation</h3>What's the initial color of the solution?
is a salt soluble in water.
dissociates into ions completely when dissolved.
.
The first test tube used to contain .
is a weak base that dissociates partially in water.
.
There's also an equilibrium between and
ions.
.
ions from
will shift the equilibrium between
and
to the right and reduce the amount of
in the solution.
The indicator equilibrium will shift to the right to produce more ions along with the colored indicator ions. The solution will show a pink color.
What's the color of the solution after adding NH₄Cl?
Adding will add to the concentration of
ions in the solution. Some of the
ions will combine with
ions to produce
.
The equilibrium between and
ions will shift to the left to produce more of both ions.
The indicator equilibrium will shift to the left as the concentration of increases. There will be less colored ions and more colorless molecules in the test tube. The pink color will fade.
<span>1,3-cylohexadiene i synthesized starting from cyclohexane in following 4 steps.
1) Free Radical Substitution Rxn: Halogenation of cyclohexane in the presence of UV yield chlorocyclohexane.
2) Elimination Rxn: Dehydrohalogenation of chlorocyclohexane yields cyclohexene.
3) Halogenation of Cyclohexene (Electrophillic Addition Rxn) gives 1,2-dihalocyclohexane.
4) Elemination Rxn: When dibromocyclohexane is treated with KOH and heated it gives 1,3-cyclohexadiene as shown below,</span>
1) Free Radical Substitution Rxn: Halogenation of cyclohexane in the presence of UV yield chlorocyclohexane.
2) Elimination Rxn: Dehydrohalogenation of chlorocyclohexane yields cyclohexene.
3) Halogenation of Cyclohexene (Electrophillic Addition Rxn) gives 1,2-dihalocyclohexane.
4) Elemination Rxn: When dibromocyclohexane is treated with KOH and heated it gives 1,3-cyclohexadiene as shown below,</span>