The order is B>C>A>E>D
Explanation: The acid strength depends on the stability of conjugate base. Also, lower the pKa of the acid greater the acidity.
HI is the strongest inorganic acid because it has pKa of -9.95 and the corresponding anion i.e I- is very stable.
Then benzene sulphonic acid is the stronger one because of the three electronegative oxygen atoms pulling electron density from the O-H bond. Also the conjugate base i.e SO3- is very stable because of resonance.
benzoic acid comes to the next where the conjugate base less stable than C but more stable than the conjugate base of E.
At last, D is the weakest acid due to it's strong O-H bond and lack of stability to the conjugate alkoxide anion.
Arrange in order of decreasing acidity. Strongest to weakest. And explain how you did this
Arrange the substances by order of acidity from weakest to strongest: CH3CH2OH CH3COOH HF C6H6
Paragraph 6. Rank the following acids in decreasing (strongest to weakest) order of acidity. Explain your choice. сон 7. Predict the product for the following reaction 1.0 2H,O, NaOHHO 3. H,0 8. Predict the product for the following reaction. ОН OH excess K.COH SOUHO 9. Provide the reagents necessary to carry out the following conversion.
Predicting Trends a point arrange the following in decreasing (fastest to slowest) rate of hydrating. Explain your arrangement. Arrange of following in order of decreasing acidity (strongest to weakest). Explain your arrangement.
Arrange the following carbolic acids in order of acidity. The strongest acid is c The second strongest is b The third strongest is a The weakest acid is d
Arrange the following carboxylic acids in order of acidity. BrCH2-COOH CH-COOH COOH O,N-CH2-COOH The strongest acid is The second strongest is The third strongest is The weakest acid is
Part A Arrange the following oxoacids in order of decreasing acid strength. Rank from strongest to weakest acid. To rank items as equivalent, overlap them. 1. HClO2 2. HClO3 3. HBrO 4. HClO Part B Arrange the following carboxylic acids in order of decreasing acid strength. 1. CHCl2COOH 2. CH2ClCOOH 3. CH3COOH 4. CH3CH2COOH Part C Arrange the following amines in order of decreasing base strength. 1. CH3NH2 2. NH3 3. NH2Br 4. (CH3)2NH
Hekp with steps please! Part A Arrange the following oxoacids in order of decreasing acid strength Rank from strongest to weakest acid. To rank items as equivalent, overlap them. Part B Arrange the following carborylic acids in order of decreasing acid strength. Rank from strongest to weakest acid. To rank items as equivalent, overlap them. Part C Arrange the following amines in order of decreasing base strength Rank from strongest to weakest base. To rank items as equivalent overlap them.
3. Rank the Lewis acidity of the following in the order of strongest to weakest Lewis acid: a. AlMe3, PMe, BMes, NMez b. FjSi™, MezSi", (Eto)Sit, H3Si
Part A Arrange the following oxoacids in order of decreasing acid strength. Rank from strongest to weakest acid. To rank items as equivalent, overlap them. 1. HClO2 2. HClO3 3. HBrO 4. HClO FYI-It is not HClO3 > HClO2 > HBrO> HClO Thanks
Part A Arrange the following oxoacids in order of decreasing acid strength.Rank from strongest to weakest acid. To rank items as equivalent, overlap them.1. HClO22. HClO33. HBrO4. HClOPart B Arrange the following carboxylic acids in order of decreasing acid strength.1. CHCl2COOH2. CH2ClCOOH3. CH3COOH4. CH3CH2COOHPart C Arrange the following amines in order of decreasing base strength.1. CH3NH22. NH33. NH2Br4. (CH3)2NH