Answer:
See explanation
Explanation:
The question is incomplete because the image of the alcohol is missing. However, I will try give you a general picture of the reaction known as hydroboration of alkenes.
This reaction occurs in two steps. In the first step, -BH2 and H add to the same face of the double bond (syn addition).
In the second step, alkaline hydrogen peroxide is added and the alcohol is formed.
Note that the BH2 and H adds to the two atoms of the double bond. The final product of the reaction appears as if water was added to the original alkene following an anti-Markovnikov mechanism.
Steric hindrance is known to play a major role in this reaction as good yield of the anti-Markovnikov like product is obtained with alkenes having one of the carbon atoms of the double bond significantly hindered.
Avoid placing themselves between moving vehicles and an immovable structure vehicle or stacked materials
Answer:
4. Option C. Pentane.
5. Option D.
Explanation:
4. Hydrocarbons are compound containing carbon and hydrogen only. Hydrocarbons are said to be saturated when they contain only carbon to carbon single bond. All alkanes are saturated hydrocarbon.
The correct answer is pentane.
5. Isomerism is the phenomenon whereby two or more compounds have the same molecular formula but different structural patterns. The compounds involved are called isomers.
A careful observation of the diagram above shows that only option D satisfied the definition of Isomerism as the two compound both have the same molecular formula as C3H8O but different structural patterns.
Note: option C does not contain isomers as Isomerism can not occur in a compound having just 1 carbon atom.
Answer:
products are copper and aluminium chloride
reactants are aluminium and copper chloride
Explanation:
products are formed at the end of a reaction
reactants are what's reacting to form the products ie the things at the start of the equation
