Concept explainers
(a)
Interpretation:
IUPAC name for the following should be identified:
Concept Introduction:
In
- Longest C chain which contains the CHO group should be named by omitting the -e ending and adding suffix -al.
- Numbering of the longest C chain should be started with giving 1st number to the C in the CHO group.
Other rules are common with the usual nomenclature.
(b)
Interpretation:
IUPAC name for the following should be identified:
Concept Introduction:
In IUPAC nomenclature aldehydes always contain -al suffix. When naming an aldehyde following steps should be followed.
- Longest C chain which contains the CHO group should be named by omitting the -e ending and adding suffix -al.
- Numbering of the longest C chain should be started with giving 1st number to the C in the CHO group.
Other rules are common with the usual nomenclature.
(c)
Interpretation:
IUPAC name for the following should be identified:
Concept Introduction:
In IUPAC nomenclature aldehydes always contain -al suffix. When naming an aldehyde following steps should be followed.
- Longest C chain which contains the CHO group should be named by omitting the -e ending and adding suffix -al.
- Numbering of the longest C chain should be started with giving 1st number to the C in the CHO group.
Other rules are common with the usual nomenclature.

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Chapter 16 Solutions
ALEKS 360 ACCESS CARD F/GEN. ORG.CHEM
- Q5: Label each chiral carbon in the following molecules as R or S. Make sure the stereocenter to which each of your R/S assignments belong is perfectly clear to the grader. (8pts) R OCH 3 CI H S 2pts for each R/S HO R H !!! I OH CI HN CI R Harrow_forwardCalculate the proton and carbon chemical shifts for this structurearrow_forwardA. B. b. Now consider the two bicyclic molecules A. and B. Note that A. is a dianion and B. is a neutral molecule. One of these molecules is a highly reactive compound first characterized in frozen noble gas matrices, that self-reacts rapidly at temperatures above liquid nitrogen temperature. The other compound was isolated at room temperature in the early 1960s, and is a stable ligand used in organometallic chemistry. Which molecule is the more stable molecule, and why?arrow_forward
- A mixture of C7H12O2, C9H9OCl, biphenyl and acetone was put together in a gas chromatography tube. Please decide from the GC resutls which correspond to the peak for C7,C9 and biphenyl and explain the reasoning based on GC results. Eliminate unnecessary peaks from Gas Chromatography results.arrow_forwardIs the molecule chiral, meso, or achiral? CI .CH3 H₂C CIarrow_forwardPLEASE HELP ! URGENT!arrow_forward
- Identify priority of the substituents: CH3arrow_forwardHow many chiral carbons are in the molecule? OH F CI Brarrow_forwardA mixture of three compounds Phen-A, Acet-B and Rin-C was analyzed using TLC with 1:9 ethanol: hexane as the mobile phase. The TLC plate showed three spots of R, 0.1 and 0.2 and 0.3. Which of the three compounds (Phen-A; Acet-B or Rin-C) would have the highest (Blank 1), middle (Blank 2) and lowest (Blank 3) spot respectively? 0 CH: 0 CH, 0 H.C OH H.CN OH Acet-B Rin-C phen-A A A <arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
