Acetone and 2-propanol are chemically interconvertible. Reduction (by the addition of the equivalent of H2) of acetone yields 2-propanol. Conversely, oxidation (by the removal of the equivalent of H2) of 2-propanol yields acetone. Is the evaporation data for these substances the same or different? If different, can you account for why this may be the case from a comparison of the Lewis structures of each substance and the IMFs present in each substance? Explain.

9) For the reaction between isopropyl 1-propyl (or 'n-propyl') ether and HBr, what are the expected main products? A) one alcohol and one alkyl bromide B) one alcohol and one alkene C) two alcohols D) one alcohol and one alkane

Use the following information to answer the question A student added bromine solution to a hydrocarbon sample that contained an isomer of C6H12 (E) in the absence of light. After shaking the sample, the student noticed that the colour of the bromine solution changed from orange to colourless. 6. An interpretation that could be made from the student's observations is that the hydrocarbon sample is and the IUPAC name of the sample could be ii. I The statement above is completed by the information in row: Row i ii A saturated B saturated hex-2-ene cyclopentane C unsaturated hex-2-ene D unsaturated cyclopentane -12 markel

Write the structural formulas for two (2) chloro-isomers that can formed from 2-methypropane (isobutene). How many sets of equivalent hydrogen are there in the compound 2-methypropane?

Compounds X and Y have the formula C6H12- Both X and Y react with one molar equivalent of hydrogen in the presence of a palladium catalyst to form 2-methylpentane. The heat of hydrogenation of X is less than that of Y. X and Y react with HBr to form a mixture of the same bromoalkanes, and they both undergo hydroboration/oxidation to give a mixture of the same alcohols. What is the structure of Y? In cases where there is more than one answer, just draw one. n. n [ ]# ChemDoodleⓇ za

Compounds X and Y have the formula C6H12. Both X and Y react with one molar equivalent of hydrogen in the presence of a palladium catalyst to form 2-methylpentane. The heat of hydrogenation of X is less than that of Y. X and Y react with HBr to form a mixture of the same bromoalkanes, and they both undergo hydroboration/oxidation to give a mixture of the same alcohols. What is the structure of Y? • In cases where there is more than one answer, just draw one. + ChemDoodle

Consider an organic molecule with the molecular formula C13H10O. a. Propose a chemically correct structure for this molecule that contains a ketone. b. Propose a chemically correct structure for this molecule that contains a functional group other than a ketone