Draw the following structures for reactants and products: 2-propylcyclohexanol + H2SO4 delta change = 2,2,3,3- tetramethylheptanal...
Provide structures for the reactants, intermediates, or products, as indicated, in the following reactions. Draw the structures in the boxes provided. NBS Br ether NBS, CCL 2. KOH, ethandl
Draw the structures of Octane and 2,2,3,3-tetramethylbutane. Their two heats of combustion are -5470 kJ/mol and -5452 kJ/mol. Explain which of the two molecules is more stable based on their heats of combustion.
1. Draw the line structures of the missing reactants or major products of the following reduction reactions. 2. Label the 13C NMR spectra provided below as benzophenone or diphenylmethanol. Draw a diagram on each spectrum showing the chemical structure of the corresponding compound and indicate which chemical shifts result from which carbon atoms. 3. Using infrared spectra that has been given below, explain which bands are most useful in distinguishing benzophenone from diphenylmethanol. What are the functional groups responsible for...
2-butene + h20 complete each reaction and draw the expanded structures of the reactants and products
What are the products of the following reactions? Draw structures of the reactants (where the chemical name is given) and products. 1. 2-methylpropene ----- H2O, H+ ------> 2. propanol ------Jone’s Reagent-----> 3. CH3CH(Cl)CH2CH3 + NaOCH2CH3 ------------> 4. acetone --------CH3MgBr, H+---------> 5. CH3CH2CH2Br + KOH ------ethanol------> 6. 2-methylpropene ------ 1. BH3 ------2. H2O2, NaOH---------> 7. benzene + 3H2 ------Ni (metal) catalyst -----------> 8. butanoic acid + ethanol ------------>
Write the balanced chemical reaction (and draw the skeletal structures of reactants and products) for the hydrogenation of cis-2,3-difluoro-2-butene.
Unambiguously identify the structures of the major products, reactants, or reagents for the following reactions, including stereochemistry when appropriate. Indicate if the reactions undergo E1, E2, SN1, or SN2 mechanism. 1. ?? H2SO4, H20o NaOCH3 CH3OH 2. CI ?? H2SO4, H20 3. t-BuOK t-BuOH 4 CI CN 5. CI XcCH.OH 6. CI
Questions: 1. Draw the structures for reactants and products for the reaction between: a. conc. HI and 2-butanol b. conc. HBr and 3-methyl-2-pentanol 1 Cori distillati
3. . Draw all the possible resonance structures: (6 points) 4. Write the products or reactants: (12 points) 3.. Draw all the possible resonance structures: (6 points) OCH3 H NO2 a. CH2 CH + H3C CH2 b. H,C 4. Write the products or reactants: (12 points) COOH 0-1 heat COOH a. HBr, leq b.
Draw bond-line structures for the following compounds. 1.) 6-tert-butyl-2,2,3,3-tetramethylnonane 2.)3-cyclohexyl-2,2,4-trimethylheptane 3.) 4-secbutyl-4,5-diisopropylnonane 4.)1,3-dicyclopentylcycloheptane