
Need help understanding why? Thanks! 9. Rank the following from most to least acidic CI COOH...
20) Rank the following Carboxyllic Acid derivatives in decreasing order (Most to Least) of reactivity towards Nucleophillic Substitution reactions? 3 Pts "NH2 II III IV More Reactive: Least Reactive 21) Match the following? 2 Pts 1) Alkynes 2) Aromatic Compounds 3) Aldehydes/Ketones 4) Carboxyllic acid derivatives A) Nucleophillic Addition Reactions B) Nucleophillic Substitution Reactions C) Electrophillic Additon Reactions D) Electrophillic Substitution Reactions
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Rank the acidity of the protons shown in the picture (from most acidic to least) I > II > III = IV IV > I = II > III IV > I > II > II I > II > IV > III What accounts for the difference between the acidity of proton (IV) and protons (I and II)? (may be more than one answer) Feature 1: energy and entropy stabilization Feature 2: energy and entropy stabilization...
could you please help me with these questions. thank you so much
45. What is the order of decreasing reactivity of aldehydes, esters and ketones? a. Aldehydes > esters >ketones b. Esters> aldehydes > ketones c. Ketones > esters > aldehydes d. Aldehydes > ketones> esters 46. Which of these will not catalyze the reaction of a weak nucleophile with the carbonyl group of an aldehyde or ketone? (Hint: Look for which is not a Lewis Acid) A) I' B)...
Rank the acidity of the following compounds in order of most acidic to least acidic. H ОН HCI HB II III IV HTML EC
4. Rank the bold-faced hydrogens for the following compounds from most acidic to least acidic. нн H H -CH3 'N CH >ICH3 COO-H Ph I II III IV V
Rank the following compounds in order of increasing acidity, putting the least acidic first. I. CH3COOH II. ClCH2COOH III. CH3CH2OH IV. ClCH2CH2OH A) III < I < IV < II B) III < IV < I < II C) II < I < IV < III D) III < I < II < IV
2. Reactivity of Aldehydes and Ketones a. Rank the following aldehydes and ketones in order from LEAST reactive to MOST reactive: н" H Н H C b. Justify your answer thoroughly in words: I ш B
why is three III more acidic than four IV
5. Which is the order from most acidic to least acidic? о CH3CH, CH3CH2OCCH COCHCH3 Il o CHICCH CH,COCH,CH, III IV (A) III > IV > II >I (B) II > IV > I > III (C) II > III > IV > 1 (D) IV > II > III > I
s (c) NH2 Rank the molecules shown in Figure 6 from H) most acidic to least acidic (example:dcba . NH2 он Figure 6 ) Which of the following is most stable carbocation? i) methyl i) primary i) secondary iv) tertiany v) Hiv are approximately equal in stability J) Which of the following is not a characteristic of most aromatic compounds like benzene? i) they are cyclic li) they are planar ii) they are resonance stabilized iv) the aikenes of the...
SE ATO 1800A . Rank the following resonance structures from MOST to LEAST stable a. III > I > II b. II > I > III c. II > III >I d. I > II > III I > III > II