+ c) FeCl3 + NH4OH Fe(OH)3 NHACI
1 answer:
The question is incomplete, the complete question is:
Write the net ionic equation for the below chemical reaction:
(c):
<u>Answer:</u> The net ionic equation is
<u>Explanation:</u>
Net ionic equation is defined as the equations in which spectator ions are not included.
Spectator ions are the ones that are present equally on the reactant and product sides. They do not participate in the reaction.
(c):
The balanced molecular equation is:
The complete ionic equation follows:
As ammonium and chloride ions are present on both sides of the reaction. Thus, they are considered spectator ions.
The net ionic equation follows:
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Answer:
Explanation:
Chemical Equations are representations of chemical reactions in terms of the symbols and formulae of the elements and compounds involved. A chemical equation usually have the reactant at the left hand side while the product is on the right hand side.
A chemical Equation is of little or no value if is not in balanced equation. When an equation is balanced , the total number of atoms of any element on the left-hand side of it must be equal to the total number of atoms of that element on the right hand side.
in the given question; we are given a word problem of chemical symbol to compute and also to balance the chemical equation.
From below; the chemical equation can be written as:
From the above equation we will notice that it is not truly balanced ; so th balanced equation can be written as:
Answer:
See explanation
Explanation:
The reaction that we are considering here is quite a knotty reaction. It is difficult to decide if the mechanism is actually E1 or E2 since both are equally probable based on the mass of scientific evidence regarding this reaction. However, we can easily assume that the methylenecyclohexane was formed by an E1 mechanism.
Looking at the products, one could convincingly assert that the reaction leading to the formation of the two main products proceeds via an E1 mechanism with the formation of a carbocation intermediate as has been shown in mechanism attached to this answer. Possible rearrangement of the carbocation yields the 3-methylcyclohexene product.
