Rank reactivity of following carboxylic acid derivatives as an electrophile from slowest (1) to fastest (5)...
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 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
Rank the reactivity of the following toward H_2SO_4/delta catalyzed dehydration, from 1 (fastest) to 4 (slowest).
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...
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
Rank (slowest to fastest) the following compounds in order of reactivity with respect to an SN2 reaction. Explain your reasoning for the ranking you propose. The compounds are 1-bromo-3-methylbutane, 1-bromo-2,2-dimethylpropane and 2-bromo-2-methylbutane.
Rank the following functions from slowest growing to fastest growing (i.e. fastest to slowest) 1 (constant) log2n (logarithmic) n (linear) n * log2 n (“n log n”) n2 (quadratic)
rank the organic chlorides from fastest to slowest based on the expected relative reactivity REACTION • The reaction between the four organic chlorides (given below) and a 1% ethanolic silver nitrate solution. HNO, R-CI + AgNO3 + CH3CH2OH Alkyl chloride 2.5 mL 2.0 mL R-OCH CH3 + AgCl + precipitate Alkyl chloride = Alkyl chloride = ra o u to
5. Rank the reactivity of the following alkyl halides (A-E) for an SN2 reaction from the fastest (1) to the slowest (5) and explain your ranking. (10 pts) H3C-Br Br Ci
Rank the following speeds from fastest to slowest. (Label the fastest as 1) 100.3 mi/hr 132.8 km/hr 0.0283 km/s 28.3 m/s