Classify the reaction below as a substitution, an elimination, or an addition. Select the single best answer. HO О О оо HCl, 4A MS OH Substitution reaction ☑ Elimination reaction Addition reaction None of the above
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- O In this step alkyne anion is alting and it is attacking cecting acting as 4 electrophile a Pla وعك Ho as a nucleophile on the genen molecule, which is Br pom 산 2-Bromo propane (26105 576 honros он 2Which represents an efficient synthetic route to go from an alkane to an alkene? O elimination with NaNH2, followed by a water workup O anti-Markovnikov hydrohalogenation, followed by elimination O radical bromination, followed by elimination O hydration, followed by elimination O hydration, followed by ozonolysis of the double bondFor the given reaction: OH ? + NaOH + NaCI + H20 Major substitution product Major elimination product Provide the IUPAC name of the major elimination product, including stereochemistry at the double bond. Answer:
- 12) Use the curved arrow formalism to show the movement of electron pairs in the following reaction and label each reactant as a nucleophile or an electrophile. CHÍNH CHỊCH, + CO Học Nha CH₂CH₂CI4. What are the products obtained from the following elimination reaction? Indicate the major product. CH;CH2CCH3 H2O CI 5. a) Determine the major product that is formed when the alkyl halide reacts with a hydroxide ion in an elimination reaction. CH;CH,CH,CH,CCH3 Br b) For the major elimination product obtained in 5a), which stereoisomer (cis or trans) is obtained in greater yield? Draw the two isomers and provide the names of the compounds.The reagents below (A-E) are used for the following questions. A H D Br PPh3 :0: H. e B :0: PPh3 (+) E H Which reagents are Wittig reagents? [Select] H Br. :0: Which Wittig reagent would yield a Z alkene when reacted when an aldehyde/ketone? [Select] C Recall the definition/structure of a Wittig reagent. Which reagents could be used to make a Wittig reagent? [Select] H
- Name of the next compound according to IUPAC rules? 10 nwn Tp ן שילה , Br of -A is buiis JailWhat is/are the missing reagent(s) (A) in the following reaction? CH3-CH₂-C-OH O H₂SO4 O CH3OCH 3 O 1)CN 2) H3O+/heat O CrO3/H+ OCH3OH/H*/heat A CH3-CH₂-C-0-CH3For each reaction, decide whether substitution or elimination (or both) is possible, andpredict the products you expect. Label the major products. chlorocyclohexane + NaOCH3 in CH3OH
- 4) Eto ₂ 5) 2-Cyclohexene-1-one O₂Et + ethylace to acetate NaOEt NaOEtThe conversion of 3 alcohols into alkenes under acidic conditions involves two cationic intermediates. For each reaction, draw the complete mechanism using curved arrows.The reactants, intermediates, final products, and all curved arrows showing bonds forming andbreaking are collectively referred to as the mechanism of a reaction. For the following reactants: a. Explain why the original statement of Markovnikov’s rule does not help in this case, but themodern restatement of Markovnikov’s rule tells you which carbon will get the X (Cl). b. Show the mechanism of the most likely addition reaction between the reactants.