(a)
Interpretation:
Correct IUPAC name for the given
Concept Introduction:
For naming an aldehyde in
IUPAC rules for naming an aldehyde:
- • The longest parent carbon chain is identified that includes the carbonyl group.
- • The parent chain name is changed by replacing the suffix “-e” with “-al”.
- • Numbering is done in a way that the carbonyl group is designated as number 1. This is not indicated in the part of the name because for aldehyde, the carbonyl carbon is always numbered 1.
- • The identity and location of substituents if any has to be determined and this information has to be added in front of the IUPAC name.
- • If the carbonyl
functional group is attached to a ring of carbon atoms, the ring is named and “-carbaldehyde” is added as suffix.
(b)
Interpretation:
Correct IUPAC name for the given aldehyde has to be assigned.
Concept Introduction:
For naming an aldehyde in IUPAC nomenclature, the suffix “-al” is added to the parent alkane name.
IUPAC rules for naming an aldehyde:
- • The longest parent carbon chain is identified that includes the carbonyl group.
- • The parent chain name is changed by replacing the suffix “-e” with “-al”.
- • Numbering is done in a way that the carbonyl group is designated as number 1. This is not indicated in the part of the name because for aldehyde, the carbonyl carbon is always numbered 1.
- • The identity and location of substituents if any has to be determined and this information has to be added in front of the IUPAC name.
- • If the carbonyl functional group is attached to a ring of carbon atoms, the ring is named and “-carbaldehyde” is added as suffix.
(c)
Interpretation:
Correct IUPAC name for the given aldehyde has to be assigned.
Concept Introduction:
For naming an aldehyde in IUPAC nomenclature, the suffix “-al” is added to the parent alkane name.
IUPAC rules for naming an aldehyde:
- • The longest parent carbon chain is identified that includes the carbonyl group.
- • The parent chain name is changed by replacing the suffix “-e” with “-al”.
- • Numbering is done in a way that the carbonyl group is designated as number 1. This is not indicated in the part of the name because for aldehyde, the carbonyl carbon is always numbered 1.
- • The identity and location of substituents if any has to be determined and this information has to be added in front of the IUPAC name.
- • If the carbonyl functional group is attached to a ring of carbon atoms, the ring is named and “-carbaldehyde” is added as suffix.
(d)
Interpretation:
Correct IUPAC name for the given aldehyde has to be assigned.
Concept Introduction:
For naming an aldehyde in IUPAC nomenclature, the suffix “-al” is added to the parent alkane name.
IUPAC rules for naming an aldehyde:
- • The longest parent carbon chain is identified that includes the carbonyl group.
- • The parent chain name is changed by replacing the suffix “-e” with “-al”.
- • Numbering is done in a way that the carbonyl group is designated as number 1. This is not indicated in the part of the name because for aldehyde, the carbonyl carbon is always numbered 1.
- • The identity and location of substituents if any has to be determined and this information has to be added in front of the IUPAC name.
- • If the carbonyl functional group is attached to a ring of carbon atoms, the ring is named and “-carbaldehyde” is added as suffix.
Want to see the full answer?
Check out a sample textbook solutionChapter 15 Solutions
Study Guide with Selected Solutions for Stoker's General, Organic, and Biological Chemistry, 7th
- I'm working on AFM data analysis of human hair sample but I'm confused on how to do itarrow_forwardPlease correct answer and don't use hand ratingarrow_forwardWhich product(s) will form under the conditions below? D Br deuterium bromide Br D OA only OB only O Conly OD only OA and D only O B and C only OA and C only B and D only A. B. C and D A B C D Br Brarrow_forward
- Please correct answer and don't use hand rating and don't use Ai solutionarrow_forwardPlease correct answer and don't use hand rating and don't use Ai solutionarrow_forwardWhat is the pH of a buffer system that contains 0.200 M Hydrocyanic (HCN) abd 0.150 M sodium cyanide (NaCN)? The pKa of hyrocyanic acid is 9.31.arrow_forward
- Show work. Don't give Ai generated solutionarrow_forwardI'm confused can you help me for steps data analysis in AFMarrow_forwardHow many equivalents are in 15.0ml of 0.12 M BA(OH)2 solution? What volume of 0.085 M HNO3 is required to reach the endpoint when titration 15.0 ml of this solution?arrow_forward
- Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co