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Murljashka [212]
3 years ago
14

What number do we use to represent the connection of a solid, liquid, or solvent?

Chemistry
1 answer:
nikklg [1K]3 years ago
4 0

Answer:Molarity tells us the number of moles of solute in exactly one liter of a solution. (Note that molarity is spelled with an "r" and is represented by a capital M.) We need two pieces of information to calculate the molarity of a solute in a solution: The moles of solute present in the solution

Explanation:

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The balanced equation is attached in the image below. The coefficients are 2, 2, blank.

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identify the reagents you would use to convert each of the following compounds into pentanoic acid: (a) 1-pentene (b) 1-bromobut
Morgarella [4.7K]

a)BH3.THF is used to convert 1-pentane to pentanoic acid and b)NaCN is used to convert Bromobutane to pentanoic acid.

a) The conversion of 1-pentane to pentanoic acid using BH3, also known as hydroboration-oxidation, is a two-step reaction involving the reaction of 1-pentane with borane (BH3), followed by oxidation of the resulting 1-pentylborane with hydrogen peroxide or other oxidizing agents.

In the first step, 1-pentane reacts with borane (BH3) to form 1-pentylborane, through a process known as hydroboration. This reaction is catalyzed by a Lewis acid, such as aluminum chloride, and proceeds via a hydride transfer from the borane to the 1-pentane.

In the second step, the 1-pentylborane is oxidized to pentanoic acid using hydrogen peroxide (H₂O₂) or other suitable oxidizing agents. The oxidation is catalyzed by an acid, such as hydrochloric acid (HCl), and proceeds via a proton transfer from the 1-pentylborane to the hydrogen peroxide. The end result is the conversion of 1-pentane to pentanoic acid.

The overall chemical reaction for the conversion of 1-pentane to pentanoic acid using borane (BH₃) and hydrogen peroxide (H₂O₂) is as follows:

1-pentane + BH₃ + H₂O₂ → pentanoic acid + H₂O + BH₂

b)The conversion of 1-Bromo butane to pentanoic acid using sodium cyanide (NaCN) proceeds via a nucleophilic substitution reaction. The reaction mechanism involves the following steps:

1. Attack of the nucleophile, NaCN, on the carbon atom of 1-Bromo butane to form a tetrahedral intermediate.

2. Loss of a proton from the tetrahedral intermediate to form a carbanion.

3. Protonation of the carbanion by water (or another proton source) to form pentanoic acid.

The overall reaction can be represented as follows:

1-Bromo butane + NaCN → Pentanoic Acid + NaBr

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2 years ago
Copper oxide is a: (Multiple Choice)
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Answer:

The answer is 5. Compound

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vladimir1956 [14]

Answer:

78.07

Explanation:

them seperatly is

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3 years ago
The antibiotic prontosil, developed by bayer pharmaceuticals in 1932, was used in saving the life of president roosevelt's son f
Alja [10]

Prontosil is a compound produced by the coupled reaction of an aryldiazonium ion and an aromatic compound.

<h3>What are diazonium compounds?</h3>

These are organic compounds in which there are ionic interactions between the azo group (-N₂⁺) and an anion X⁻.

The general structure is RN₂⁺X⁻.

  • R is the lateral chain that might be an aromatic ring, among other options.
  • N₂⁺ is the azo group
  • X⁻ is the anion

The azo group characterizes as being unstable and reactive. This property is because one of the N atoms has a positive charge.

-N⁺≡ N

<h3>What is the coupling reaction of aryldiazonium compounds?</h3>

Aryldiazonium salt reactions can occur in two ways,

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Coupling reactions are the aromatic electrophilic substitution, where the aryldiazonium ion acts as an electrophile for an activated aromatic compound to attack it.

The coupling reaction occurs at the azo group level.

In the exposed example,

  • the benzene ring with sulfur bonded to oxygen atoms is the coupling component
  • the benzene ring with NH₂ and the azo group is the diazonium ion

In the attached files you will find the drawings.

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