<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>
Answer:
The resulting solution is basic.
Explanation:
The reaction that takes place is:
First we <u>calculate the added moles of HNO₃ and KOH</u>:
- HNO₃ ⇒ 12.5 mL * 0.280 M = 3.5 mmol HNO₃
- KOH ⇒ 5.0 mL * 0.920 M = 4.6 mmol KOH
As <em>there are more KOH moles than HNO₃,</em> the resulting solution is basic.
Answer:
A. tungsten
Explanation:
Tungsten is a material which high melting point ie. does not melt easily incase of high temperature
Answer:
Explanation:
% yield = (actual yield / theoretical yield) X 100
For this question,
% yield = (150g/ 162 g) X 100 = 92.6%