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- a H2O H2SO4 2 Br2 (4) (5)Reagents Available g. CO, HCI, CUCI/AICI3 h. CH3CH2CH2COCI, AICI3 i. BrCH2CH2Br, Он j. CH3CH2CI, AICI3 k. RCO3H I. H3O* a. CH2=CHCH,CI, AICI3 b. CH2B12, OH c. CH3CH2COCI, AICI3 d. H2, Pt e. NBS, CCI4 f. K* tBuO Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol). Select reagents from the table in the order that you wish to use them, i.e. aced; do not include punctuation or spaces If more than one route exists, choose the shorter one; in no case will a synthesis require more than 5 steps.a) b) c) d) CI H3CH₂CC CH CO + CH3MgBr 1. 2 eq. PhMgBr 2. H3O+ 1. NaNH, 2. PhCHO 3. H₂O* Azculi + 1. ether 2. H30* -Br r
- Draw the structure of (Z)-1-bromo-1-chloro-1-butene. • Consider E/Z stereochemistry of alkenes. • You do not have to explicitly draw H atoms. AAVII ? ChemDoodle [F ⓇA B C D E 1. NaBH4 2. H3O+ 1. CH3MgBr 2. H3O+ 1. (CH3)2CuLi 2. H3O+ 1. CH3Li 2. H3O+ 1. (CH3CH2)2CuLi 2. H3O+Account for the regioselectivity and stereoselectivity observed when this compound is treated with Hg(OAc)2 in H₂O Use wedge and hash bonds ONLY when needed to show reaction stereochemistry. . If the reaction produces a racemic mixture, just draw one stereoisomer.
- 1) Classify the following dienes and polyenes as isolated, conjugated, cumulated or some combination of these classifications. a) (db) wold mwe eing o niolionsih odt to d ot slon d) 1,3,5-cyclohexatriene (benzene) c) 1,3,6-cyclooctatrieneDraw all the constitutional isomers formed by monohalogenation of(CH3)2CHCH2CH3 with Cl2 and hv.H ll PTSCluster.pptcap.loc hapter X MasteringChemistry: Chapter 4 A X ew?offset3Dnext&assignmentProblemID=170497302 Part A What is the IUPAC name for the molecule shown? Enter the IUPAC name for the molecule. - View Available Hint(s)