i need help ls i thank its book 500 grams
Answer:
In the presence of UV light, ethane will react with bromine in a substitution reaction. UV light is the condition under which the reaction will occur so it is written above the arrow in the chemical equation. As the reaction proceeds, the intensity of the re-brown colour of the bromine water decreases.
Answer:
When naming molecular compounds prefixes are used to dictate the number of a given element present in the compound. ” Mono-” indicates one, “Di-” indicates two, “Tri-” is three, “Tetra-” is four, “Penta-” is five, and “Hexa-” is six, “Hepta-” is seven, “Octo-” is eight, “Nona-” is nine, and “Deca-” is ten.
For the reaction Cl₂(aq) + 2 Br⁻(aq) ⇒ 2Cl⁻(aq) + Br₂(aq), Chlorine (Cl) is the oxidizing agent because it gains an electron.
<h3>What is the oxidizing agent?</h3>
In a redox reaction, the oxidizing agent is the one that gains electrons, causing the other element to oxidize.
Let's consider the following redox reaction.
Cl₂(aq) + 2 Br⁻(aq) ⇒ 2Cl⁻(aq) + Br₂(aq)
The corresponding half-reactions are:
Reduction: 2 e- + Cl₂(aq) ⇒ 2Cl⁻(aq)
Oxidation: 2 Br⁻(aq) ⇒ Br₂(aq) + 2 e-
Which best describes the oxidizing agent in this reaction?
- Bromine (Br) is the oxidizing agent because it gains an electron. NO. Br is the reducing agent.
- Bromine (Br) is the oxidizing agent because it loses an electron. NO. Br is the reducing agent.
- Chlorine (Cl) is the oxidizing agent because it gains an electron. YES.
- Chlorine (Cl) is the oxidizing agent because it loses an electron. NO. Cl gains electrons.
For the reaction Cl₂(aq) + 2 Br⁻(aq) ⇒ 2Cl⁻(aq) + Br₂(aq), Chlorine (Cl) is the oxidizing agent because it gains an electron.
Learn more about oxidizing agents here: brainly.com/question/9064518
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Substitution Reactions are those reactions in which one nucleophile replaces another nucleophile present on a substrate. These reactions can take place via two different mechanism i.e SN¹ or SN². In SN¹ substitution reactions the leaving group leaves first forming a carbocation and nucleophile attacks carbocation in the second step. While in SN² reactions the addition of Nucleophile and leaving of leaving group take place simultaneously.
Example:
OH⁻ + CH₃-Br → CH₃-OH + Br⁻
In above reaction,
OH⁻ = Incoming Nucleophile
CH₃-Br = Substrate
CH₃-OH = Product
Br⁻ = Leaving group
Organic reactions are typically slower than ionic reactions because in organic compounds the covalent bonds are first broken, this breaking of bonds is a slower step, while, in ionic compounds no bond breakage is required as it consists of ions, so only bond formation takes place which is a quicker and fast step.
