4. Design a synthetic scheme using any reagents and reactions that have been discussed in CHEM2402. Onlyreactions and reagents from CHEM2402 will be considered.iv)i)مللii)b) Design a synthetic scheme using the reagents given for the following two reactions. All reagents are used foreach reaction scheme and in each case, a reagent can be used more than once. Take the necessary time tocomplete this question.2 eq.Br2 eq.BrH₂/ Lindlar's catalyst Br₂/CH₂Cl₂2 однHNaH H3O+/H₂OH₂/ Lindlar's catalyst PCC/CH₂Cl₂NaHH H3O+/H₂OCH₂Br

In part (iv), ketones are formed generally from an alkene or an alcohol. So reducing this given…

Answered: 4. Design a synthetic scheme using any…

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...

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Practice Problems 3. Explain why 4-methyl-3-penten-2-one absorbs at 314 nm, quite a bit higher than both butadiene and hexatriene. Your answer must explain how Lmax relates to molecular structure. 4. Explain which reaction would be faster and why. You need to use the rate law data to recognize which mechanism is at play. Br. Nal Reaction 1: acetone substrate A Rate = k [substrate A] Nal Reaction 2: acetone Br Br substrate B Rate = k [substrate B]
Identify the best reagents to complete the following reaction. Options are included.
5. Our textbook gives two reactions that result in anti-Markovnikov additions with alkenes. i. ii. iii. The first is hydroboration forming an anti-Markovnikov Draw the single mechanistic step of the "syn" addition which determines the anti- Markovnikov addition. I The second, the radical addition of HBr to an alkene, has a critical propagation step which determines the addition selectivity. Draw this step below.
5. Propose a synthesis of each of the following compounds using the indicated starting material. You may use any organic compounds, inorganic compounds, organometallic compounds, or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. a. H3C steps гумон OH (racemic) F3C CI F3C Ph b. H3C. CH3 H3C CH3 steps C. steps CH3 NH2 (racemic)
Can you please check my work on the retrosynthetic analysis ... I had to provide the needed reagents to perform the syntheses... My answers are in BLACK thank you
step-wise and mechanisms please.
Which of the following is a limitation of the Friedel-Crafts reaction? Select one: O A. The carbocation electrophile can potentially undergo an unwanted rearrangement prior to its bonding to the aromatic ring. OB. Poly-alkylation products form when aromatic reactant and alkylating agent are mixed together in comparable amounts. OC. A Friedel-Crafts reaction fails when the aromatic starting compound contains a moderately or strongly deactivating group. OD. All of the above choices are limitations of the Friedel-Crafts reaction.
Which sequence of reactions would be best for achieving the transformation shown below?
Chemistry Is there anyone who can provide this pericyclic rxn mechanism? Problem 161. The following transformations entail an "apparent" methyl migration. Address the questions posed below. Part A. Provide a mechanism for the transformation of 1 to 2. I represents an 180 label. Classify all pericyclic processes should they intervene. Part B. Provide a mechanism for the transformation of 3 to 4. Classify all pericyclic processes should they intervene. Me Me Me Me Me Me, heat x=28=8. heat Me 1 Mé
What is a successful synthetic strategy for this transformation? OH O 1. XS MeMgBr, 2. H2O 1. SOCI2, 2. CH3Br O 1. DMSO, C202C12, 2. MeMgBr, 3. H3O+ O NaBH4 OH
Can i get help with these problems
b Search results for write complet * Illinois State University : CHE 22 X > aromatic nitration assignment.p x A reggienet.illinoisstate.edu/access/content/attachment/ale286d3-b539-436a-9dae-4501422658c6/Assignments/97c80ba1-8f18-42f9-bfad-7694cfc0. E U4SD.Org Imported From IE M TalentEd 4 News & Announce. * U4SD Intranet New Tab TAC O Zoom O EAC ТАС O JunpRope W Illinois REALTORS®. >> aromatic nitration assignment.pdf 1 / 2 + 100% ОН KMNO4 H3C- CH3 H,SO4, H2O 1 С. H OH H,PO, D. Mc 4 O v i 1:11 ТАС

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4. Design a synthetic scheme using any reagents and reactions that have been discussed in CHEM2402. Only reactions and reagents from CHEM2402 will be considered. iv) ملل Br Br