
Concept explainers
(a)
Interpretation:
Using trivial names where appropriate, the name for the given molecule is to be written.
Concept introduction:
Benzene derivatives have one or more substituents attached to the benzene ring. In such compounds, the root name is benzene. The ring is numbered so that the substituents attached to it get the lowest locator numbers. Prefixes and locator numbers are used for writing the number and type of substituents. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root.
(b)
Interpretation:
Using trivial names where appropriate, the name for the given molecule is to be written.
Concept introduction:
For a molecule that has more than one double bond or triple bond, the name must indicate the number of double bonds or triple bonds present as well as their locations. To name the molecule with multiple double/triple bonds, establish the root as the longest carbon chain or the largest carbon ring that contains the greatest number of entire
Trivial names are also commonly used for substituents containing
(c)
Interpretation:
Using trivial names where appropriate, the name for the given molecule is to be written.
Concept introduction:
Benzene derivatives have one or more substituents attached to the benzene ring. In such compounds, the root name is benzene. The ring is numbered so that the substituents attached to it get the lowest locator numbers. Prefixes and locator numbers are used for writing the number and type of substituents. If the substituents attached to a benzene ring are complicated, it is easy to treat the benzene ring as a substituent instead of a root. Alkenes, alkynes, and benzene derivatives have trivial names. Trivial names are also commonly used for substituents containing
(d)
Interpretation:
Using trivial names where appropriate, the name for the given molecule is to be written.
Concept introduction:
For a molecule that has more than one double bond or triple bond, the name must indicate the number of double bonds or triple bonds present as well as their locations. To name the molecule with multiple double/triple bonds, establish the root as the longest carbon chain or the largest carbon ring that contains the greatest number of entire
Trivial names are also commonly used for substituents containing

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Chapter B Solutions
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
- Draw the stepwise mechanism for the reactionsarrow_forwardPart I. a) Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone b) Pinacol (2,3-dimethyl, 1-3-butanediol) on treatment w/ acid gives a mixture of pina colone (3,3-dimethyl-2-butanone) and 2, 3-dimethyl - 1,3-butadiene. Give reasonable mechanism the formation of the products Forarrow_forward3. The explosive decomposition of 2 mole of TNT (2,4,6-trinitrotoluene) is shown below: Assume the C(s) is soot-basically atomic carbon (although it isn't actually atomic carbon in real life). 2 CH3 H NO2 NO2 3N2 (g)+7CO (g) + 5H₂O (g) + 7C (s) H a. Use bond dissociation energies to calculate how much AU is for this reaction in kJ/mol.arrow_forward
- Part I. Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone and answer the ff: Pinacol (2,3-dimethyl, 1-3-butanediol) on treatment w/ acid gives a mixture of pina colone and (3,3-dimethyl-2-butanone) 2,3-dimethyl-1,3-butadiene. Give reasonable mechanism the formation of the products Forarrow_forwardShow the mechanism for these reactionsarrow_forwardDraw the stepwise mechanismarrow_forward
- Draw a structural formula of the principal product formed when benzonitrile is treated with each reagent. (a) H₂O (one equivalent), H₂SO₄, heat (b) H₂O (excess), H₂SO₄, heat (c) NaOH, H₂O, heat (d) LiAlH4, then H₂Oarrow_forwardDraw the stepwise mechanism for the reactionsarrow_forwardDraw stepwise mechanismarrow_forward
- Part I. Draw reaction mechanism for the transformations of benzophenone to benzopinacol to benzopinaco lone and answer the ff: a) Give the major reason for the exposure of benzophenone al isopropyl alcohol (w/acid) to direct sunlight of pina colone Mechanism For b) Pinacol (2,3-dimethy 1, 1-3-butanediol) on treatment w/ acid gives a mixture (3,3-dimethyl-2-butanone) and 2, 3-dimethyl-1,3-butadiene. Give reasonable the formation of the productsarrow_forwardwhat are the Iupac names for each structurearrow_forwardWhat are the IUPAC Names of all the compounds in the picture?arrow_forward
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