a.
Interpretation:
Name the given compound.
Concept introduction:
The nomenclature of
Naming Aldehydes:
Aldehydes have at least one hydrogen attached to the carbonyl carbon atom.
The IUPAC naming of an aldehydes is obtained by replacing the final "e" on the name of the parent hydrocarbon with "al".
The common name of the aldehyde is substituted for "oic acid" at the end of parent hydrocarbon chain.
For example:
Naming Ketones:
Carbonyl carbon atom attached to the two oxygen atoms.
The IUPAC name of a ketones are obtained by replacing the "e" on the end of the parent hydrocarbon with "one".
Only few ketones have common name.
For example:
b.
Interpretation:
Name the given compound.
Concept introduction:
Naming Aldehydes:
Aldehydes have at least one hydrogen attached to the carbonyl carbon atom.
The IUPAC naming of an aldehydes is obtained by replacing the final "e" on the name of the parent hydrocarbon with "al".
The common name of the aldehyde is substituted for "oic acid" at the end of parent hydrocarbon chain.
For example:
Naming Ketones:
Carbonyl carbon atom attached to the two oxygen atoms.
The IUPAC name of a ketones are obtained by replacing the "e" on the end of the parent hydrocarbon with "one".
Only few ketones have common name.
For example:
c.
Interpretation:
Name the given compound.
Concept introduction:
Naming Aldehydes:
Aldehydes have at least one hydrogen attached to the carbonyl carbon atom.
The IUPAC naming of an aldehydes is obtained by replacing the final "e" on the name of the parent hydrocarbon with "al".
The common name of the aldehyde is substituted for "oic acid" at the end of parent hydrocarbon chain.
For example:
Naming Ketones:
Carbonyl carbon atom attached to the two oxygen atoms.
The IUPAC name of a ketones are obtained by replacing the "e" on the end of the parent hydrocarbon with "one".
Only few ketones have common name.
For example:
d.
Interpretation:
Name the given compound.
Concept introduction:
Naming Aldehydes:
Aldehydes have at least one hydrogen attached to the carbonyl carbon atom.
The IUPAC naming of an aldehydes is obtained by replacing the final "e" on the name of the parent hydrocarbon with "al".
The common name of the aldehyde is substituted for "oic acid" at the end of parent hydrocarbon chain.
For example:
Naming Ketones:
Carbonyl carbon atom attached to the two oxygen atoms.
The IUPAC name of a ketones are obtained by replacing the "e" on the end of the parent hydrocarbon with "one".
Only few ketones have common name.
For example:
Want to see the full answer?
Check out a sample textbook solutionChapter 16 Solutions
Organic Chemistry (8th Edition)
- Name each of the following structures.arrow_forwardPlease don't provide handwriting solutionarrow_forwardWhich one of the following statements about arene oxides is FALSE? O The NIH shift is what makes arene oxides carcinogenic. O Ring opening of an arene oxide can afford an addition product and/or a rearranged product. O Large polycyclic aromatic hydrocarbons such as benzo[a]pyrene are especially susceptible to arene oxide formation. The NIH shift mechanism was discovered at the National Institutes of Health. O Cytochrome P450 is the powerful biological oxidant that epoxides an arene to give an arene oxide.arrow_forward
- optically active 2- butanole slowly becoms racemic whem treated with with dilute acid > explain whyarrow_forwardd-Glucuronic acid is found widely in plants and animals. One of its functions is to detoxify poisonous HO-containing compoundsby reacting with them in the liver to form glucuronides. Glucuronides are water soluble and therefore readily excreted. Afteringestion of a poison such as turpentine or phenol, the glucuronides of these compounds are found in the urine. Draw thestructure of the a- and b-glucuronides formed by the reaction of b-d-glucuronic acid and phenol.arrow_forward( do all with explanation plzarrow_forward
- 2. Compound A, C;H100 , is one of the basic building blocks of nature. All steroids and many other naturally occuring compounds are built from compound A. Spectroscopic analysis of A yields the following information: IR: 3400 cm-'; 1640 cım- IH NMR: 1.63 & (3 H, singlet); 1.70 ô (3 H, singlet); 3.83 6 (1 H, broad singlet); 4.15 8 (2 H, doublet, j = 7 Hz); 5.70 ô (1 H, triplet, ) = 7 Hz) (a) How many double bonds and/or rings does A have? (b) From the IR spectrum, what is the identity of the oxygen-containing functional group? (c) What kinds of protons are responsible for the NMR absorptions listed ? (d) Propose a structure for A.arrow_forwardWhich of the following hydrolysis reaction is incorrectarrow_forwardDo it asaparrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
- EBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENT