True, The products obtained by the acid-catalyzed hydration of 1-methylcyclohexene and 1-methylenecyclohexane are identical.
Methylcyclohexane is a colorless liquid with a faint, Benzene-like smell. it's miles used as a solvent and to manufacture organic chemical substances.
The extra fantastically substituted alkene is 1-methylcyclohexene, given that there's only one H substituent at the double bonded carbons. that is the predominant product. whilst injected repeatedly. methylcyclohexane proved to be poisonous for the liver, heart, and kidney at a high dose. absolutely the toxic dose changed into. at the same time as the no discovered destructive effect stage. The substance exerted little impact on the reproductive system.
Methylcyclohexane, as a aspect of a mixture, is usually dehydrogenated to toluene, which will increase the octane rating of gas. It may be produced by means of a Wittig response or a reaction with a reagent from cyclohexanone. it can additionally be synthesized as a side made of the dehydration of 2-methylcyclohexanol into 1-methylcyclohexene.
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If one were to match the ratio of atoms of the elements found in this molecular formula of artificial sweetener it would be :
Carbon - 7 atoms
Hydrogen - 5 atoms
Nitrogen - 1 atom
Oxygen - 3 atoms.
Answer:
See explanation
Explanation:
The question is incomplete, however, I found an example of this question on another site, so, I'm going to explain to you how to do it basing on this example, and then, apply it in your case. In the picture 1, is the example, and picture 2 is the solution.
Now, this type of reaction is known as the "<em>Williamson Ether synthesis"</em><em> </em>and the overall of this, is a reaction that involves an alkoxyde ion with an primary alkyl halide like this:
RO- + R'X ------> ROR' + X-
This is a Sn2 reaction, and it's really fast.
Following the example in picture 1, the result is in picture 2. Hope this can help you.