(a)
Interpretation:
The name of the following aldehyde is to be determined.
Concept Introduction:
While naming the
(b)
Interpretation:
The name of the following aldehyde is to be determined.
Concept Introduction:
While naming the aldehydes as per the IUPAC nomenclature, the naming of the compounds is done by adding a suffix-al at the end of the name. Firstly, one will find the longest chain that contains the -CHO group and then change the -e ending of the parent alkane chain to -al suffix. Then, the numbering of the chain or the ring is done in such a way so as to put the -CHO group at carbon no. 1 followed by omitting this number from the name. Thereafter, apply all other rules of nomenclature as usual.
(c)
Interpretation:
The name of the following aldehyde is to be determined.
Concept Introduction:
While naming the aldehydes as per the IUPAC nomenclature, the naming of the compounds is done by adding a suffix-al at the end of the name. Firstly, one will find the longest chain that contains the -CHO group and then change the -e ending of the parent alkane chain to -al suffix. Then, the numbering of the chain or the ring is done in such a way so as to put the -CHO group at carbon no. 1 followed by omitting this number from the name. Thereafter, apply all other rules of nomenclature as usual.
(d)
Interpretation:
The name of the following aldehyde is to be determined.
Concept Introduction:
While naming the aldehydes as per the IUPAC nomenclature, the naming of the compounds is done by adding a suffix-al at the end of the name. Firstly, one will find the longest chain that contains the -CHO group and then change the -e ending of the parent alkane chain to -al suffix. Then, the numbering of the chain or the ring is done in such a way so as to put the -CHO group at carbon no. 1 followed by omitting this number from the name. Thereafter, apply all other rules of nomenclature as usual.
(e)
Interpretation:
The name of the following aldehyde is to be determined.
Concept Introduction:
While naming the aldehydes as per the IUPAC nomenclature, the naming of the compounds is done by adding a suffix-al in the end of the name. Firstly, one will find the longest chain that contains the -CHO group and then change the -e ending of the parent alkane chain to -al suffix. Then, the numbering of the chain or the ring is done in such a way so as to put the -CHO group at carbon no. 1 followed by omitting this number from the name. Thereafter, apply all other rules of nomenclature as usual.
Want to see the full answer?
Check out a sample textbook solutionChapter 16 Solutions
General, Organic, and Biological Chemistry - 4th edition
- Draw the organic products formed when each alkyne is treated with two equivalents of HBr.arrow_forwardWhat product is formed when each alkene is treated with HCl?arrow_forward18. Identify the lactone formed by the following hydroxy carboxylic acid. A. A B. B C. C D. D OH OH & & A) B) C) D)arrow_forward
- 2. How many different ß-hydroxyaldehydes and ß-hydroxyketones, including constitutional isomers and stereoisomers, are formed upon treatment of a mixture of acetone and benzaldehyde with base? a. b. 2 c. 3 d. 4arrow_forwardDraw the products formed when each alkene is treated with HCl.arrow_forwardCan you answer and explain d-f?arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning