Which class of addition reaction is represented by the transformation below: O dihydroxylation O hydrohalogenation O halohydrin formation ○ hydration O hydrogenation O ozonolysis O halogenation Br
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- Which of the following reactions uses a safer solvent according to green chemistry? halogenation C alkylation C reduction of a ketone with sodium borohydride C halohydrin formationWhich of the following organic compound is an aldehyde? CH3CH2CHO O CH2 = CHCI O CH3COC2H5 O CH3CH2CIAldehydes and ketones react with thiols to yield thioacetals, just as they react with alcohols to yield acetals. Draw the structure of the third intermediate in this reaction. H* catalyst .SCH3 + 2 CH3SH SCH3
- Which 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 bond610) For the reaction between isopropyl 1-propyl (or 'n-propyl') ether and HBr, which type of reaction best matches the expected products? A) Acid-catalyzed dehydration B) Nucleophilic substitution reaction C) Ether cleavage reaction D) Nucleophilic addition-elimination reaction
- Draw the structures of the missing reactant, reagent, or major organic product(s)Draw the two reactants used to form the following compound, label the nucleophile and the electrophile, and using arrows show the points of attack of the nucleophile on the electrophile that enables the formation of the heterocyclic product.What is the the nucleophilic substitution product?
- A single alkyl bromide reactant theoretically yields either of the given products, depending on the reaction conditions. Draw the structure of the alkyl bromide compound. alkyl bromide (one compound only) CH, ОН СH O DMSOWhich class of addition reaction took place in the transformation below: halogenation ozonolysis O hydrohalogenation O dihydroxylation O hydrogenation O hydration OH OHcomplete the synthesis cyclohexane to 1R,2R 2 bromocyclohexanol