Put the following molecules in order towards nucleophilic addition (1 = most reactive). Explain your order.
Put the following molecules in order towards nucleophilic addition (1 = most reactive). Explain your order....
Accessibility Mode Print P Find E Imme 7) A compound C7H140 has a strong peak at 1710 cm. Its 'H NMR spectrum consists of three singlets in the ratio of 9:3:2 at 8 1.0, 2.1, and 2.3 respectively. Identify the compound. 8) Put the following molecules in order towards nucleophilic addition (1 = most reactive). Explain your order Acetone Tert-butylmethyl ketone Perfluroacetone Formaldehyde GIVE FEEDBACK TO Options for clas
Question 28 Which of the following compounds is most reactive towards a nucleophilic addition reaction? o e H Н H 1 11 IV II III IV V FO F10 FB F7 F6 F5 F4 F2 F3 * A & @ $ % 5 7 LO 8 3 4 N
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 carbonyl-containing compounds in order of reactivity towards nucleophilic attack. Most Reactive to least reactive. 3-methylpentanoyl chloride, acetic anhydride, hexyl propanoate, N,N-diphenylethanamide, butanedial, and propanone.
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution Most reactive acetyl chloride hexyl propanoate Least reactive acetic anhydride propionamide
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic attack. Most reactive acetyl chloride propionamide benzoic anhydride isopropyl benzoate acetaldehyde propanone Least reactive
1. Explain why aldehyde A is more reactive to nucleophilic addition reactions than ketone B.
1. Explain why aldehyde A is more reactive to nucleophilic addition reactions than ketone B.
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
Rank the molecules in decreasing order of reactivity towards addition of a nucleophile to the most electrophilic sp2-hybridized carbon. Most reactive Least reactive (CH3)2C-0 (CHalzCeO'H (CHalzC-NH