Rate of hydration increases if electron withdrawing groups present near C=O . This creates more electrophilic carbon and H2O ca attack the electrophilic carbon of C=O
Hence order base on this is
A > B > C > D
Carboxylic acid acidity increases if electron withdrawing groups present adjacent to COOH .
D> B > C > A
Predicting Trends a point arrange the following in decreasing (fastest to slowest) rate of hydrating. Explain...
Arrange the following in order of decreasing reactivity (fastest to slowest) toward electrophilic aromatic substitution: Arrange the following in order of decreasing reactivity (fastest to slowest) toward electrophilic aromatic substitution: COOH бо ob 6
Arrange in order of decreasing acidity. Strongest to weakest. And explain how you did this
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.
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
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
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
Question 6 Based on your lab report, arrange the following alcohols from fastest to slowest positive Lucas test. (HINT: Lucas test is time dependent test) НЫС. а) ОН CH3 ОН b) он с
Question 19 8 pts Rank the following according to the rate of Sn1 reactivity. (greatest = fastest, least = slowest) Br OH 1. II. III. 1> | > III II >> III > | > 1 Question 20 8 pts Rank the following according to acidity. (greatest = strongest, least = weakest) H
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.
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