The question is incomplete, complete question is:
Study this chemical reaction:
Then, write balanced half-reactions describing the oxidation and reduction that happen in this reaction.
Oxidation:
Reduction:
Answer:
Oxidation taking place in given reaction :
Reduction taking place in given reaction;
Explanation:
Redox reaction is defined as the reaction in which oxidation and reduction reaction occur side by side.
Oxidation reaction is defined as the chemical reaction in which an atom looses its electrons. The oxidation number of the atom gets increased during this reaction.
Reduction reaction is defined as the chemical reaction in which an atom gains electrons. The oxidation number of the atom gets reduced during this reaction.
In the given reaction, iron(II) ions are getting reduced and zinc metal is getting oxidized to zinc(II) ions.
Oxidation :
Reduction ;
Answer:
The chemical equation needs to be balanced so that it follows the law of conservation of mass. A balanced chemical equation occurs when the number of the different atoms of elements in the reactants side is equal to that of the products side.
Answer:
2.17 e -14
Explanation:
A strong acid like HCl ionize 100 % in water so [H3O+] = 0.46 M
[OH-] = Kw / [H3O+]
= 1.0 e -14 / 0.46
= 2.17 e -14
Answer:
Explanation: A yellow precipitate o lead iodide is formed. see equation of reaction below: →
Th PbI2 is the insoluble yellow precipitate
Resonance, leaving group, carbonyl carbon delta+, and steric effect is the most crucial variables that affect the relative reactivity of a functional group containing a carbonyl in an addition or substitution process.
Discussion:
1. Carbonyl Carbon Delta+: The carbonyl group becomes more electrophilic and accelerates nucleophilic assault when the carbonyl carbon delta+ is bigger.
2. Resonance: When the carbonyl is transformed into the tetrahedral adduct, it may be lost. Loss of resonance increases the energy of the transition state for this nucleophilic assault because resonance has the function of stabilizing. Therefore, a carbonyl functional group's resistance to nucleophilic attack increases as resonance in the group increases in importance.
3. Leaving group: Tetrahedral adduct fragmentation is encouraged by a better LG.
4. Steric effects: The nucleophilic attack on carbonyl carbon is delayed when sterically impeded.
Learn more about carbonyl here:
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