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Rama09 [41]
3 years ago
5

What is the substitution reaction plzz answer ​

Chemistry
1 answer:
Nimfa-mama [501]3 years ago
3 0

Answer:

it is a reaction whereby one or more reactants of the reaction are changed or replaced .

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What hydrocarbons burn completely in an excess of oxygen, the products are
Sindrei [870]
The right answer for the question that is being asked and shown above is that: "C) carbon monoxide and carbon dioxide" hydrocarbons burn completely in an excess of oxygen, the products are <span>C) carbon monoxide and carbon dioxide</span>
3 0
3 years ago
Read 2 more answers
On the reaction below, label the BSA, BSB, CA, and CB. CH3COOH + H2O → CH3COO– + H3O+
Ostrovityanka [42]

Answer:

Acid(BSA) = CH₃COOH

Base (BSB) = H₂O

Conjugate base (CB) = CH₃COO⁻

Conjugate acid (CA) = H₃O⁺

Explanation:

Equation of reaction;

CH₃COOH + H₂O → CH₃COO⁻ + H₃O⁺

Hello,

From my understanding of the question, we are required to identify the

1) Acid

2) Base

3) conjugate acid

4) conjugate base in the reaction

Acid (BSA) = CH₃COOH

Base (BSB) = H₂O

CA = conjugate acid = H₃O⁺

CB = conjugate base = CH₃COO⁻

7 0
3 years ago
Based on the information in the passage, what is true of gases?
luda_lava [24]
1: True
2: True
3: False
4: False

(Question 2 might not be true, not sure)
7 0
3 years ago
Indicate whether each of the following statements is correct or incorrect.1)Every Bronsted-Lowry acid is also a Lewis acid2)Ever
Hunter-Best [27]

Answer:

1) correct

2) incorrect

3) correct

4)incorrect

Explanation:

1) A Lewis acid is a substance that accepts a nonbonding pair of electrons.

A Bronsted-Lowry acid is a substance that donates a proton H⁺

Since the donation of a proton involves the acceptance of a pair of electrons, every Bronsted-Lowry acid is also a Lewis acid.

2)A Lewis acid not necessarily needs to have a proton to be donated.

3) Conjugated acids of weak bases are strong acids and conjugated acids of strong bases are weak acids.

4)K⁺ comes from a strong base, therefore is does not have an acidic behaviour.

4 0
3 years ago
Compound a is an alkene that was treated with ozone (followed by dms) to yield only 4-heptanone. Draw the major product that is
olga nikolaevna [1]

Alkenes on reacting with ozone results in the formation of ozonide which undergo reductive  cleavage in presence of dimethyl sulfide to form carbonyl compounds (aldehyde or ketone). Whereas in presence of hydrogen peroxide it undergoes oxidative cleavage to form carboxylic acids or ketones.

Since, A alkene yields 4-heptanone only on treatment with ozone and DMS thus, it implies that both the chains on the side of the double-bond are similar the product is 4-heptanone that means the double bond is present between the chains at the 4th carbon. Therefore the structure of compound A is 4,5-dipropyloct-4-ene.

The reaction is as shown in the image.

The reaction of A with m-CPBA (meta-perchlorobenzoic acid) followed by aqueous acid H_3O^{+} is shown in the image.

m-CPBA (meta-perchlorobenzoic acid) is a peracid and forms epoxides on reacting with alkenes.

5 0
3 years ago
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