The following presented reaction scheme lead to the synthesis of which major product trom benzene, assumng separaton of produch s posse 1 NaOH Product Prodact 2. H0 Fe OA Meta Chlorophenol OR para ChloroSulfenic acid OC Para Chlorophenol ODMela-chloroanline
Q: 10. Provide a synthesis for the following molecule. S
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Q: The following presented reaction scheme lead to the synthesis of which major product from benzene,…
A: Para-chlorophenol formed as a product. So option C is correct.
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Q: ini.H O a. 1. NaOH; 2. H₂O* b. 1. LiAlH4; 2. H₂O* OC. BH 3 THF O d. 1. NaBH4; 2. H3O* O e. 1. DIBAH;…
A: We will discuss the speciality of each reagent.
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A: The above transformation can be achieved as follows:
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Q: The following presented reaction scheme lead to the synthesis of which major product from benzene,…
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A: Since you have posted multiple questions, we are entitled to answer the first only.
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A: -NH2=ortho para director -NO2=meta director -Cl is ortho para director.
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Q: Show how you would Synthesize the following Compounds, storting with benzene Or toluene and ony…
A: Given starting material: Benzene
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A: There is the conversion of o-hydroxybenzoic acid to o-hydroxyacetophenone.
Q: 10. Provide a synthesis for the following molecule. `SH
A: Introduction: We have to make products for the following reaction.
Q: 3. Complete the following reactions by giving products in each case. KMnO4 1) LIAIH, 2) H3O* NH2OH…
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Q: ZI
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- Li ナ >ntermedinte Theoretical yicld |-og R4-093/mol Haw mych benzaldchyde B necded to Synthe Sze O-5009 4 diphenymethanol according to The 9bove equatuin -Draw the structure of the expected major organic product for each of the following five (5) questions. Specify stereochemistry clearly, if relevant. A. CH3 excess Na NH3 (1) H3C-C=C- -CH3 H, cat. Ni,B H3C-C=C С. PB33 H3C° HO, CH D. PhS Na product from reaction 1C Е. OH CH3 H;PO4 ""CH3 B.The following presented reaction scheme lead to the synthesis of which major product from benzene assuming separation of products is possible? 1 NaOH CI. Product Product HSO 2 H,0 FeCl OA Meta-Chlorophenol U& para-ChloroSulfenic acid 6C Para-Chlorophenol 0O Mela chioroaniline
- itagram video by Mrbioo N X D Time-ManiMo 2019 X E New ta Content Owt21Oine teaching and te O https://cvg.cengagenow.com/ilr/takeAssignment/takeCovalentActivity.dolocatorasigrment-take Draw the structure(s) of the major organic producti(s) of the following reaction. NH2 Trace of acetic acid ethanol • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right comer. Separate multiple products using the + sign from the drop-down menu. C P opy aateCyclohexene plus 1) Hg(OAc)2, H2O; 2) NaBH4; yields __________. HO2CCH2CH2CH2CH2CO2H a cyclic diketone cyclohexyne cyclohexanol OHCCH2CH2CH2CH2CHOBb any.edu/webapps/assessment/take/launch.jsp?course_assessm m制 Туре: MC QUESTION 10 Which of the following alkynes does not form the ketones shown on hydration with H2O, H2SO4 and H9SO4. There may be more than one correct answer. IESTION 11 ut tho following conversion?
- Provide the major organic product of the reaction shown. NV L Draw the molecule on the canyas by choosing buttons from the Tools (for bonds), t [1] A OH 4' 1. NaH эсе 2. CH₂CH₂CH₂CH₂I H: 120 EXP. CONT L Marvin JS ? ** I U ZOS CI BrIn each reaction box, place the best reagent and conditions from the list provided. 1) Br 2) 3) DEET (the active ingredient in over the counter insect repellant) 4) 5) Answer Bank Mg. Et,0 CH,CH,OH НСООСH, H,CO НСООН NH(CH,CH,),(2 equiv.) Br,, FeBrz CH,COOH HN(CH,CH,), (1 equiv.) NaNH, H,0+ CH,CH,NH, CO, CH,CH, Br SOC, NaCNIdentify the structure of the product in the following reaction. Provide a suitable mechanism with proper justification OTs TMS Cs,Co, NHTS Tetracyclic Compound C23H21NO2S Ph Me Of 18-crown-6 Mol. wt. 375
- Cambridge International AS Level Chemistry ot boe slo plgmes s al snsdismonooli End-of-chapter questions 1 1-bromobutane will undergo reactions when heated, as shown by reactions A and B. ot dwab on s bl auoltse s boaub svsd 20 swoll gab ods-suai la yel snoso sdr ssiganm n2 monl gnivims noiteibar VU luad CH;CH,CH,CH,Br B CH;CH,CH,CH,OH CH;CH,CH=CH, 90u S1s 2O1D Isdh tuo gomia sli ni qu dgid tod a guch pecoue For reactions A and B give the reagents used in each case. b Reaction A was repeated using 1-iodobutane instead of 1-bromobutane. Explain any difference in the rate of reaction observed. p bas- od mon c What type of organic reaction is A? d Show the mechanism for reaction A. e Reaction A was repeated with 2-bromo-2-methylpropane instead of 1-bromobutane. i Name the organic compound formed. elle ii The mechanism of the reaction with 2-bromo-2-methylpropane differs from the mechanism of smitas nosd asd i anol reaction A. Describe how the mechanisms differ. f What type of reaction is…(d) With reference to the following reaction scheme: Me tBu 13 Reagent(s)? Me!!!. OH E noitesu cheq lo 19van A tBu 146 jqmolts nA (6) lobis boaaono gniau bauogmos prins bns to ouxims ni besteni batles M bon Jelsistum woler (1) Draw cyclohexanone 13 in the lowest energy chair conformation. (ii) Suggest an appropriate reagent to achieve this stereoselective reduction of cyclohexanone 13 to cyclohexanol 14 and explain your choice of reagent (curved arrow mechanisms are not required).14) What is the major organic product of each of the following reactions? + H,N-NH-Ph H* + 2 CH,OH + LIAIH(O-t-Bu); + (CH;CH,),CULİ