Chapter 7: Q14P (page 324)
State the hybridization of each carbon atom in the hydrocarbon structures in problem 12.
Short Answer
The hybridization of each carbon is assigned as given below-
Chapter 7: Q14P (page 324)
State the hybridization of each carbon atom in the hydrocarbon structures in problem 12.
The hybridization of each carbon is assigned as given below-
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Get started for free(a) Write the molecular formula of acetylsalicylic acid (see Fig. 7.34a).
(b) An aspirin tablet contains 325 mgacetylsalicylic acid. Calculate the number of moles of that compound in the tablet.
When an ester forms from an alcohol and a carboxylic acid, an oxygen atom links the two parts of each ester molecule. This atom could have come originally from the alcohol, from the carboxylic acid, or randomly from either. Propose an experiment using isotopes to determine which is the case.
A compound C3H6O has a hydroxyl group but no double bonds. Write a structural formula consistent with this information.
(a) The insecticide methoprene (see Fig. 7.32d) is an ester. Write the structural formulas for the alcohol and the carboxylic acid that react to form it. Name the alcohol.
(b) Suppose that the carboxylic acid from part (a) is changed chemically so that the OCH3 group is replaced by a hydrogen atom and the COOH group is replaced by a CH3 group. Name the hydrocarbon that would result.
The naphthalene molecule has a structure that corresponds to two benzene molecules fused together:
The electrons in this molecule are delocalized over the entire molecule. The wavelength of maximum absorption in benzene is 255 nm. Will the corresponding wavelength in naphthalene be shorter or longer than 255 nm?
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