Why do gases have fluidity
2 answers:
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Answer:
It has been drawn and uploaded as an attachment. Please download it to see the structure.
Explanation:
The product formed as a result of the reaction of cyclohexene with H2 in presence of Pt (platinum) can be described as catalytic hydrogenation. Catalytic hydrogenation is defined as the process of hydrogen addition in the presence of a catalyst, which in this case is platinum.
Note that Cyclohexene (alkene) is a hydrocarbon molecule represented by the chemical formula, C6H10 .
It consists of a double bond. During the hydrogenation reaction, the alkene undergoes an addition reaction to give alkane which is a saturated hydrocarbon as the product.
The first step in order to derive the product is to draw the chemical structure of cyclohexene and identify the double bond present in it.
The final product can be derived by replacing the double bond with the single bond and satisfying all the valences of the carbon atom. The final product structure has been drawn and uploaded as an attachment. Please download it to see the structure.
Ans:
The structure of the cyclohexane thus, formed has been shown as follows with all the hydrogen atoms:
Answer:
Explanation:
In this case we want to know the structures of A (C6H12), B (C6H13Br) and C (C6H14).
A and C reacts with two differents reagents and conditions, however both of them gives the same product.
Let's analyze each reaction.
First, C6H12 has the general formula of an alkene or cycloalkane. However, when we look at the reagents, which are HBr in ROOR, and the final product, we can see that this is an adition reaction where the H and Br were added to a molecule, therefore we can conclude that the initial reactant is an alkene. Now, what happens next? A is reacting with HBr. In general terms when we have an adition of a molecule to a reactant like HBr (Adding electrophyle and nucleophyle) this kind of reactions follows the markonikov's rule that states that the hydrogen will go to the carbon with more hydrogens, and the nucleophyle will go to the carbon with less hydrogen (Atom that can be stabilized with charge). But in this case, we have something else and is the use of the ROOR, this is a peroxide so, instead of follow the markonikov rule, it will do the opposite, the hydrogen to the more substituted carbon and the bromine to the carbon with more hydrogens. This is called the antimarkonikov rule. Picture attached show the possible structure for A. The alkene would have to be the 1-hexene.
Now in the second case we have C, reacting with bromine in light to give also B. C has the formula C6H14 which is the formula for an alkane and once again we are having an adition reaction. In this case, conditions are given to do an adition reaction in an alkane. bromine in presence of light promoves the adition of the bromine to the molecule of alkane. In this case it can go to the carbon with more hydrogen or less hydrogens, but it will prefer the carbon with more hydrogens. In this case would be the terminal hydrogens of the molecules. In this case, it will form product B again. the alkane here would be the hexane. See picture for structures.
