I am drawing the structure as they
are already there. I am mentioning them with explanation.
We can compare the pKa values of these pairs to say the acidity.
Smaller the pKa values stronger the acid.
a) Second compound in first pair is more acidic due to presence of nitro group. Amide group will increase the pKa so first structure is less acidic.
b) Second compound in second pair is more acidic due to presence of electron-withdrawing group. Presence of ester group in the first structure makes it less acidic and pKa will be more.
c) First compound in the third pair is more acidic due to presence of aldehyde group. Presence of aldehyde group always increase the acidity than cyano group.
d) In the fourth pair of compounds, one has a diester group and one has acyl chloride group. Presence of ester group makes the structure less acidic than acyl chloride hence first structure is more acidic than second one.
e) In the pair mentioned here one structure have aldehyde and one have ketone group in adjacent of alpha hydrogen as difference. Presence of aldehyde makes the Second compound more acidic in nature.
1. Which alpha hydrogen in each pair of compounds is more acidic (5 І в -...
Which of the following compounds is most acidic? І п ш у
Question-5. Which one of the following alcohols is most acidic? ОН ОН ОН IV А. В. с. І || III IV
For each pair of species, predict which is the stronger base? 5. Он or 1. 2. or В в NH NH (a) (b) 6. Rank the following from most stable to least stable. 2. 3. 4. Нас Н-с O H -н CH H CH,сH, сн,сн CH,CH 7. Which cation would be the most stable? А. В. C. D. What is the order of increasing contribution to the resonance hybrid? 8. CF3 ÇF3 CF3 I II III
Which of the following molecules has the most acidic alpha hydrogen(s)? - So Lion H OEt OH II III IV H Н EIO OEt HO OH V VI VII VIII
Which of the following compounds is more acidic? Provide a detailed explain for c. your answer. (1+4 points) II
Predict which member of each pair is more acidic, and explain the reasons for your predictions. (a) cyclopentanol or 3-chlorophenol (b) cyclohexanol or cyclohexanethiol (c) cyclohexanol or cyclohexanecarboxylic acid (d) butan-1-ol or 2,2-dichlorobutan-1-ol
Part I.Part II. Of the following pairs of compounds, select the more basic in each pair in water (you should be selecting four compounds to properly answer this question).
1) Which is the least acidic hydrogen in the compound shown? 2) Which is the most acidic hydrogen in the compound shown? 1) Which is the least acidic hydrogen in the compound shown? IV I a) I b) II c)III d) IV e) v 2) Which is the most acidic hydrogen in the compound shown? IV a) l b) ll c) III d) IV e) V
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
OMe and and NH2 .NH2 ОMe and CI А C В For each pair of compounds above, state whether they are the same compound (S), enantiomers (E), diasteriomers (D), constitutional isomers (C), or completely different (X) А C B