need all answeres ASAP List the carboxylic derivatives in order of reactivity from most to least...
rank the following carboxylic scos derivatives in decreasing order (most to least) of reactivity towards nucleophilic substitution. Question 5 Incorrect Mark o out of 1 p Flag question Rank the following carboxylic acid derivatives in decreasing order (most to least) of reactivity towards nucleophilic substitution. Select one: a. I > IV > Ill>llx b. ll > III > IV> a. l> 111 11> IN d. 1 > IV>II> e. I>l> 111 11
stion 17 What is the order of reactivity of the following carboxylic acid derivatives from most reactive to least reactive towards nucleoph 22 Ester Acid chloride Acid anhydride Amido Carboxylate anion [a] [b] (c) (d (e) Specified Answer for a Specified Answer for b Specified Answer for c Acid chloride Acid anhydride Carboxylate anion Ester Specified Answer for d Specified Answer for e Amide
Part A Rank the following carboxylic acid derivatives in order of decreasing reactivity. Rank from most to least reactive. To rank Items as equivalent, overlap them Reset Help walio ΝΗ: Most reactive Least reactive Submit Request Answer 2 A 31 If you wanted to directly synthesize the following molecule: NH which of these acid chloride derivatives could you potentially use as a starting material without converting it to another derivative first? Check all that apply. Submit Request Answer Provide Feedback
The reactivity sequence of carboxylic acid derivatives (acyl halides, anhydrides, acids, esters, amides) changes with the substituent. Acyl chlorides are most reactive, amides are least reactive. 1) Explain in detail why the reactivity changes in that sequence, 2) Where do carboxylates fit in that sequence and why? How does that impact on the way carboxylic acid reactions need to run? 3) Where do thioesters, RC(-O)SMe and acyl phosphates, RC(-O)OPO2OR fit in that sequence. Explain your decision The reactivity sequence of...
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
Chem 202, Fall 2019 Homework Packet 9 (Carboxylic Acid Derivatives) 2. Reactivity of Carboxylic Acid Derivatives a. Rank the following carboxylic acid derivatives in order from LEAST reactive to MOST reactive when they undergo nucleophilic acyl substitution reactions: — '— ' la do lan loons obe OCH3 b. Justify your answer thoroughly in words. Your explanation should include, if applicable, definitions and explanations that cover leaving group ability, conjugate acid strengths, pKa values, etc. 4. Amide Formation Mechanism: Draw the...
The reactivity of carboxylic acid derivatives depends on their leaving group. Rank the following molecules from most reactive (-best LG) to least reactive (worst LG). Input a ranking number in the box next to each structure (1-best LG). CH₃ id
18. Order the carboxylic acid derivatives from most reactive to least reactive towards nucleophilic substitution Br (A) 3 1>2>4 (B) 2>1>43 (C) 4>2>3>1 (D) 1>3>2>4 (E) 3>2>1>4
4. Rank these carboxylic acid derivatives in order of least reactive to most reactive towards nucleophilic acyl substitution reactions. (4 points) i لیل OMe NH2 1 2 3 Least Most
Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reactions (most to least reactive from left to right in the answer) yucuruit pun Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reaction (most to least reactive from left to right in the answer): ei ole C>A>D>B A>C>D>B A>C>B>D C>A>B>D