Circle the most reactive and square the least reactive.
Circle the most reactive and square the least reactive. - Circle the most reactive and square...
Question 14 (2 points) Which of the following compounds is the most reactive dienophile in a Diels- Alder reaction? соосн, NO2 соосн соосн. OB) II OD) IV
Diels-Alder CN Reaction CN diene dienophile D. 1. 03, -78°C "H H' 2. Zn/H2O 4. Circle all aromatic compounds: (2 points)
Rand these dienophiles in decreasing order of reactivity in the Diels-Alder reaction. Most reactive = 1, least reactive = 4.
Provide the product structure of the Diels-Alder reaction show below. Identidy the respective substrates with either diene or dienophile labels circle the correct answer 1) Provide the product structure of the Diels-Alder reaction show below. Identify the respective substrates with either diene or dienophile labels-circle the correct answer below the substrate. (2 pts) 25 °C OCH3 OH Diene Diene or or Dienophile Dienophile c yclohex-3- eneccbaylc a 2) True or False: Butadiene is an (1 pt) easily handled liquid that...
18, 22, 23 16) What diene and dienophile would react to give the product below? diere 17) Which of the following compounds is the most reactive dienophile in a Diels-Alder reaction with 1,3-butadiene? A) CH-CHOCH B) CH2-CHCHO C) CH3CHCHCH3 D) (CH3CH2 5) C .CH 18) Using resonance structures, explain the regiochemistry observed in this reaction OCH H.CO heat 19) Provide the major organic product of the following reaction H.CO ÇOCH H.COM 20) Provide the major organic product of the following...
1) Provide the product structure of the Diels-Alder reaction show below. Identify the respective substrates with either diene or dienophile labels-circle the correct answer below the substrate. (2 pts) Diene Diene or Dienophile or Dienophile
Multiple Choice, T/F Questions 1. Which of the following are TRUE (T) or FALSE (F) regarding Diels-Alder reactions? a) The reaction involves syn addition. _b) The reaction occurs in multiple steps. c) The reaction is a [4+2] A cycloaddition. d) The adduct formed fasted is the exo isomer. e) Electron donating groups activate the diene. f) Electron withdrawing groups activate the dienophile. 2. The compound at the right does not undergo Diels-Alder reaction because: a) ring systems cannot function as...
This is an organic chemistry question regarding the Diels-Alder reaction. The problems are 16.22 and 16.18. I would like to know if I did these correctly. If I did not, could someone help me go through the process? er reaction Conjugation, Resonance and Dienes Chapter 16 dienophile react in a Diels-Alder CH3 C. 16.18 Draw the product formed when each diene and Problem 16.18 COOCH3 15 Specific Rules Governing the Diels-Alder Reaction 16.13A Diene Reactivity Rule [1] The diene can...
4 Which of the fotlowing is the most reactive carhosylie acid derivative A) ester D) anhydride 2 nitrile D) acid chloride E) amide 11) Typically, amides will hydrolyse under A) stronger B) more dilute conditions than esters C) milder D) less vigorous E) more saline 12) 1-Methyleyclopentanol is classified as A) a primary aloohol B) a secondary alcohol C) a tertiary alcohol D)a phenol E) an enol 13. For a diene to undergo a Diels-Alder reaction it must: be substituted...
order these substrates from most to least reactive in an SN1 reaction. CI د بل لا ) 6 ) )