<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:
A
Explanation:
Because Rainwater can get acidic because of the carbonic acid that it contains
Explanation:
21. The given molecule for cracking is tetradecane.
On cracking it forms one mole of decane (C10H22) and two moles of ethene gas.
The chemical equation is shown below:

22. The essential condition for the formation of an ester is the reaction of alcohol and acid in presence of concentrated sulfuric acid.
Thus among the given options, the first option is the correct one.
23. Isomers of butanol are shown below:
It is 2-butanol.
The position of -OH group changes to the second carbon.
Answer:
Empirical Formula N2O6Sr Strontium Nitrate
Explanation:
N=13.2% O=45.4% Sr=41.4%
Answer:
a) heat it from 23.0 to 78.3
q = (50.0 g) (55.3 °C) (2.46 J/g·°C) =
b) boil it at 78.3
(39.3 kJ/mol) (50.0 g / 46.0684 g/mol) =
c) sum up the answers from the two calculations above. Be sure to change the J from the first calc into kJ
Explanation: