What is the effect of Cl on the acidity of carboxylic acids?

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queen_honey_blossom answered 2 years ago

How do you rate the acidity from highest to lowest for acids ( carboxylic acids and...

How do you rate the acidity from highest to lowest for acids ( carboxylic acids and alcohol) ? How do you rate nucleophilic strength ? How do you rate the reactivity of a carbonyl receiving a backside attack? how do you rate the boiling points of carboxylic acids, amides, esters, alcohols rank solubility of carbaldehyde , carboxyilic acid ester in water

The relative acidity between carboxylic acids has been used as a means for determining the electron-withdrawing...

The relative acidity between carboxylic acids has been used as a means for determining the electron-withdrawing or electron-donating abilities of substituents. a) The pKa of phenyl acetic acid is 4.31, making it a stronger acid than acetic acid. Is the Ph group electron-donating or electron-withdrawing in this case? b) The Ph group is a mild o,p-director in EAS reactions. Is the Ph group electron-donating or electron-withdrawing? If the answer contradicts your answer from part a, provide an explanation. c) 4-Methoxybenzoic...

Give the IUPAC name for each of the following carboxylic acids.

Why doesnt the 2,4 DNPH test work for carboxylic acids?

Which of the following is not correct about carboxylic acids? Which of the following is not...

Which of the following is not correct about carboxylic acids? Which of the following is not correct about carboxylic acids? Carboxylic acids do not form intermolecular H-bonding with water. Carboxylic acids are very polar molecules. There is intermolecular H-bonding between the molecules of carboxylic acids. Carboxylic acids with higher molar mass (molecular weight) are not much soluble in water.

Carboxylic Acids. Lipids are a macromolecule we need to survive and many of them happen to...

Carboxylic Acids. Lipids are a macromolecule we need to survive and many of them happen to contain carboxylic acids. Choose one lipid - could be a particular steroid, fatty acid, or tri-glyceride and discuss its structure and potential reactivity. please cite on source using APA citation format.

The table of diprotic acids below shows how the acidity of the 1st proton is always...

The table of diprotic acids below shows how the acidity of the 1st proton is always much higher than the acidity of the second proton.Thus, the pH of the solution is dominated by the equilibrium for the loss of the 1st proton. Compound Ka1 Ka2 H2CO3 4.3 X 10-7 5.6 X10-11 H2S 8.9 X 10-8 1.0 X 10-19 H2Te 2.3 X 10-3 1.6 X 10-11 H2SO3 1.7 X 10-2 6.4 X 10-8 What is the pH for a 1.12 M...

Please compare two synthetic approaches toward carboxylic acids. A. Grignard reagent approach; B. Nitrile approach. What...

Please compare two synthetic approaches toward carboxylic acids. A. Grignard reagent approach; B. Nitrile approach. What are the advantages and disadvantages of each method?Please compare two synthetic approaches toward carboxylic acids.

1. List the major nomenclature rules for carboxylic acids, give an example (draw structure and give...

1. List the major nomenclature rules for carboxylic acids, give an example (draw structure and give name) 2. Explain the two major influences on the acidity of the O-H bond in carboxylic acids 3. Describe specific reagents used to oxidize and reduce aldehydes and ketones, provide an example of each (4 total) 4. Draw the mechanism for the Grignard reaction

Both aqueous HCl and HNO3 are strong acids (equal acidity in water); yet CuO will dissolve...

Both aqueous HCl and HNO3 are strong acids (equal acidity in water); yet CuO will dissolve more easily in 1 M HCl than in 1 M HNO3. What accounts for this difference?

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