Most reactive dienophile in diels alder reaction is the one having electron withdrawing groups as they decrease energy of dienophile orbitals.
In I , one NO2 ( electron withdrawing group) is there
In II, one COOCH3 (electron withdrawing group) is there
In III, two COOCH3 (electron withdrawing group) are there
In IV, one CH3 (electron releasing group) is there
More are electron withdrawing groups on dienophile, higher is its reactivity. So answer is C option III.
Question 14 (2 points) Which of the following compounds is the most reactive dienophile in a...
Question 29 (2 points) Which one of the following dienophiles is least reactive in the Diels-Alder reaction? NO OCH H3CO TI IV O a) IV Oы) і OI d) III Question 30 (2 points) Which of the following are possible products of the reaction shown? hv NBS Br Br III IV a) I, II, III and IV Ob) I, III and IV O I, II and III O d) I and II
Circle the most reactive and square the least reactive. - Circle the most reactive and square the least reactive dienophile in a Diels-Alder Reaction (4 points). لا کر = م ه م - Circle the most reactive and square the least reactive diene in a Diels-Alder Reaction (4 points).
Question 21 (2 points) Which one of the following dienophiles is least reactive in the Diels-Alder reaction? OCH ОСН, Нco. IV a) b) III Oc)!! d) IV Question 22 (2 points) Which of the molecules below would be the expected product for the hydrogenation of the following alkene with Na and liq. NH3? Na NH v III IV a) Ob) II Oc) d) v Question 23 (2 points) Identify the final product for the following reaction. 1. BH3, THE 2....
Question 31 (2 points) What are the expected major products of the reaction sequence shown below? 1. O 2. H70 OH o OH 11 III IV v Oa) I and IV ob) I and II oc) I, III and IV od) II, III and IV Question 32 (2 points) Which one of the following dienophiles is least reactive in the Diels-Alder reaction? NO, phony HCO 11 IV Oa) III ob) IV Oc) 1 od) 11
3) Which of the following compounds is the most reactive dienophile in a Diels-Alder reaction with 1,3-butadiene? A) CH2CHOCH3 B) CH2CHCHO C) CH3CHCHCH3 D) (CH3)2CCH2 E) CH2CH2 5) Which of the following fails to form benzoic acid when heated with chromic acid? A) 1-phenylethanol B) 2-phenylethanol C) 2-phenylheptane D) 2-methyl-2-phenylheptane E) 1-phenylheptanol 11) How can the following synthesis be carried out? A) HCOOH; HNO3/H2SO4 B) CH3Cl/AlCl3; HNO3/H2SO4; H2CrO4, heat C) CH3Cl/AlCl3; H2CrO4, heat; HNO3/H2SO4 D) HNO3/H2SO4; CH3Cl/AlCl3; H2CrO4, heat E)...
Question 7 (2 points) Which of the following dienes can undergo the Diels-Alder reaction? II III IV a) 11 Ob) III Oc) Od IV Question 8 (2 points) How would you use 'H NMR spectroscopy to distinguish between the following compounds based on the benzene ring protons? II O O a) Benzene protons for I show up between 6.0 - 7.0 ppm and Il between 7.0 - 8.0 ppm Ob) Benzene protons for I show up between 7.0 - 8.0...
Question 15 4 pts Consider the diene and dienophile required to make each of the following Diels-Alder adducts. Which of these would be created the most rapidly (hint: numbering helps). OH OH HO. HO, HO. HO" HO: ОН A B C D E OD O C 0 A OB
Question 21 (2 points) Which of the following dienes can undergo the Diels-Alder reaction? III IV Oa) III ob) 11 Oc) od) IV Question 22 (2 points) Predict the product(s) of the following reaction. нег ROOR Oa) HBr addition at the alkene position following Markonikov's rule Ob) HBr addition at the alkene position following Anti-Markonikov's rule Oc) H20 addition at the alkene position following Anti-Markonikov's rule od) H20 addition at the alkene position following Markonikov's rule
Question 13 (2 points) Predict the reactants for the following Diels- Alder product: OB 0: co 0:41 oa) IV ob) Oc) III od) 11 Question 14 (2 points) Calculate the degree of unsaturation for CgH9N04. oa) 8 ob) 6 OC) 9 od) 4
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