b) Fill in the gaps by drawing the structures of the missing reagents, intermediates and/orproducts of the following electrophilic aromatic substitutions. Chemical formulas have beenadded for guidance. .Step 1Step 2CH3HNO.1.CH;NO2C;H3NPd/CNO23124CH3Brz FeBrC3H;Bro6Using resonance structures, justify whether the acetyl group of compound 5 will direct thebromination reaction to the meta or ortho/para positions

The electrophilic substitution reaction is the significant reaction of aromatic benzene ring which…

b) Fill in the gaps by drawing the structures of the missing reagents, intermediates and/or products of the following electrophilic aromatic substitutions. Chemical formulas have been added for guidance.. Step 1 Step 2 CH3 ENO, H2 1. CH;N Pd:C NO2 2 4 CH3 Br FeBr C3H;Bro Using resonance structures, justify whether the acetyl group of compound 5 will direct the bromination reaction to the meta or ortho/para position.

b) Fill in the gaps by drawing the structures of the missing reagents, intermediates and/or products of the following electrophilic aromatic substitutions. Chemical formulas have been added for guidance.. Step 1 Step 2 CH3 ENO, H2 1. CH;N Pd:C NO2 2 4 CH3 Br FeBr C3H;Bro Using resonance structures, justify whether the acetyl group of compound 5 will direct the bromination reaction to the meta or ortho/para position.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

starting from acetylene and alkyl halides not longer than 4 carbon atoms, show the synthesis of 3-octanol and a ketone. indicate the reagents in each step.you may use more than one mole of the reactants
Which of the following compounds can be converted to an alkyl lithium compound in one step by reacting with lithium metal? i) ii) Br OH iii) iv) Br Он .COOH O Only i O Only two of the structures O Only ii O All of the structures O Only i
For each of the given reactions, pick the correct description and the correct reagent.
Use benzenonium resonance forms to explain why the methoxyl group (-OCH3) is o, p-directing in electrophilic aromatic substitution reactions.
Draw the principal organic product for the reaction of 2-bromohexane with lithium in diethyl ether, followed by formaldehyde in diethyl ether, and then followed by dilute acid. Click and drag to start drawing a structure. X A G P
CH3 Br,/FeBr3 C3H;BrO 5 Using resonance structures, justify whether the acetyl group of compound 5 will direct the bromination reaction to the meta or ortho/para positions.
Briefly describe the role of this molecule as it relates to bees. Propose Two reasonable syntheses of this molecule from benzene. there are multiple syntheses possible (the first proposed synthesis required twelve steps) HO. OH
4
Give typed explanation of all subparts Provide an IUPAC name for the following compounds. You may use benzoic acid instead of benzenecarboxylic acid
Substitutions on aromatic rings are generally carried out by electrophilic substitution, but for the synthesis of phenolic compounds and alkoxy benzene it is carried out by nucleophilic substitution, explain why this is so .
Draw the organic product obtained by hydroboration-oxidation of each of the following alkenes: (a) trans-2-pentene, (b) 2-tert-butyl-3,3-dimethyl-1- butene, and (c) 1-methylcyclohexene. Having done this, draw the product of the acid-catalyzed hydration of these same alkenes. How do the reaction products differ?
Specialized reagents and their acronyms: MCPBA= meta-chloroperbenzoic acid; HOAC = acetic acid, NaOAc = Sodium Acetate; Ph= phenyl = C6H5-; P(Ph)3 = triphenyl phosphine; NBS = N- bromosuccinimide, PBR3, SOCI2, AlCl3, FeBr3, H2SO4, Li, Na, Mg, Br2, CrO3, LDA = lithium diisopropylamide, PCC = pyridinium chlorochromate, KO-C(CH3)3, LAH = LIAIH4, (sia)2BH = disecondary isobutyl borane, KMNO4, HIO4 = periodic acid %3D %3D %3D %3D %3D write the missing reagents and solvents over the arrows. Some transformation require multiple steps. In some cases there will be multiple arrows. Br Br