An experimenter uses 1-heptanol instead of cyclohexanol for the reaction of (Oxidation of Cyclohexanol with Hypochlorite). What would be the major product of the reaction
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An experimenter uses 1-heptanol instead of cyclohexanol for the reaction of (Oxidation of Cyclohexanol with Hypochlorite).
What would be the major product of the reaction?
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- Draw the structures of the following compounds. (Includes both new and old names.)(a) triphenylmethanolProvide another method for preparation of cyclohexene from another compound except cyclohexanol (provide the equation only)?compare these two reaction (a) and (b) which both produces alkene. explain what are the major differences between these two reactions ?
- Why does the solubility of carboxylic acids decreases with the increase in size of alkyl groups? a.)This is because of the equal polarity and hinderance provided by the large alkyl groups to the COOH group from involving in the hydrogen bonding with solvent molecules. b.)This is because of the reduced polarity and hinderance provided by the large alkyl groups to the COOH group from involving in the hydrogen bonding with solvent molecules. c.)This is because of the increased polarity and hinderance provided by the large alkyl groups to the COOH group from involving in the hydrogen bonding with solvent molecules. d.)This is because of the hinderance provided by the large alkyl groups to the COOH group from involving in the hydrogen bonding with solvent molecules.COMPLETE THE TWO REACTIONS BELOWWhat class of the reaction is the "synthesis of hexyI acetate reaction" an example of? What about the starting material suggest that it follows the reaction pathway?
- The addition of water to aldehydes and ketones occurs rapidly, although it is not thermodynamically favored. What would be the product for the reaction above? Hint: Think of the self-ionization of water and the polarity of the carbonyl group.b) Which of these two would you expect to have the higher boiling point? Why? hexanal c) Write "most" under Write "least" under benzonitrile pentanoic acid compound which will react with Cly/FeCl, most easily. compound which will be least reactive toward Cly/FeCl. ethylbenzene chlorobenzene(a) What functional group is undergoing a transformation in the reaction? (b) What functional group is it being transformed into (in the final product)?
- Considering the stoichiometry of the reaction (balance the equation!), what is the net oxidation state difference of the carbons in benzophenone going to benzopinacol? Remember that you have to calculate the oxidation state of the carbons in the product (benzopinacol) and subtract the oxidation state of the carbons in the reactants (benzophenones). The shortcut is to only calculate the oxidation states of the carbons that seem to have changed their bonding. Give a whole number answer with no units. hv OH Ph Ph OH Ph' Ph' Ph Ph OH Answer: -1Considering the stoichiometry of the reaction (balance the equation!), what is the net oxidation state difference of the carbons in benzophenone c to benzopinacol? Remember that you have to calculate the oxidation state of the carbons in the product (benzopinacol) and subtract the oxidation state of the carb the reactants (benzophenones). The shortcut is to only calculate the oxidation states of the carbons that seem to have changed their bonding Give a whole number answer with no units. OH hv Ph Ph OH Ph Ph Ph Ph OH Answer:Complete the following reaction. Thank you!