↓ Draw the major elimination and substitution products formed in this reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Ignore any inorganic byproducts. Br NaOH heat Draw One of the Major Products I + > esc
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- Predict the product(s) for the following reaction. O ll + enantiomer I OI ||| OH O IV OH CN OH + enantiomer || 1. NaCN 2. H₂O CN "ОН + enantiomer ||| IV CN CNGive IUPAC names for the following structures. When appropriate, abbreviate ortho (o), meta (m), and para (p), no italics, if you elect to use these terms. CH₂CH₂CHCHCHSCHCH₂ I T CH₁ CH₂ 1st structure: CH3 CH3 I 2nd structure: Submit Submit Answer Try Another Version OCH3 CH₂CCH₂ OCH3 10 item attempts remainingStarting from the wedge-and-dash structure below (sighting down the indicated bond), rotate the back carbon to provide the structure in the conformation that will be capable of an E2 elimination. R/S stereochemistry is graded. # O H3C H Drawing > CI ||||| H Atoms, Bonds and Rings Tap a node to see s
- The AH° values of each compound is given below as kJ/mol. Calculate the entaphy change (AH) value of the following reacti on? 2CaOg) + 2SO2 (g + Ozg) →2 CasO41) -635.5 -296.9 0.0 -1432.7 (kJ/mol) A) 500.3 kJ B) -500.3 kJ С) -1000.6 kJ D) 2365.1 kJ E) -1094.1 kJces to access important values if needed for this question. Complete the equation for the following reaction by drawing a structural formula for the missing organic product. CH3CH2NH2 H20 CH,CH,C-OH • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Draw cations and anions in separate sketchers. P. opy aste C. [F Visited CH4 M) M) M) ChemDoodle Submit Answer Retry Entire Group 5 more group attempts remainingThe following Wittig reactions may produce a mixture of alkene stereoisomers. Write the products for each of the reactions and indicate the stereoisomers if any. || Ph,P CH3 + ? (1) LOME (2) R N. Ph,P=CH,R' Me
- a Draw the structure of the intermediate (I) for the reaction below. Hg(O2CCH3)2 NaBH4 Product CH;OH H3C • Use the wedge/hash bond tools to indicate stereochemistry where it exists. If the reaction produces a racemic mixture, just drawv one stereoisomer.Rank the following alkenes in order of increasing rate of hydrogenation. 11 OI<|||< IV < II <|| < |||R'R?CHOH-CR°R* R'R?C=CR®R* What should orientation of each substituent in reactant to convert it into product alkene? What is importance of their specific orientation?What is (are) the major organic product(s) obtained from the following reaction? Br2 O (2R,3R)-dibromobutane meso-2,3-dibromobutane O (2S,3S)-dibromobutane O Racemic mixtureDraw the major elimination and substitution products formed in this reaction. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore any inorganic byproducts. H₂O Br Draw One of the Major Products + > a heat Draw One of the Major ProductsConsider the following mechanism of reaction: CH3 CH, CH3 CH;C CH, + H-CI CH;CCH, + C: → CH;CCH, tert-butyl cation CI tert-butyl chloride In this reaction: The alkene and the carbocation intermediate are both nucleophilic HCl and CI" are both nucleophilic The alkene and HCI are both electrophilic The carbocation and CI" are both electrophilic The alkene and CI" are both nucleophilic AMeving to another question will save this responseSEE MORE QUESTIONS