
Concept explainers
Interpretation:
The parent chain has to be chosen and numbered correctly for the given compound.
Concept Introduction:
All the molecules have their unique names. These names must be known in order to communicate. But remembering all the chemical names is impossible as there are many numbers of molecules. To avoid this, the
Stereoisomerism | Substituents | Parent | Unsaturation | Functional Group |
Stereoisomerism indicate if the considered molecule has any stereocenters are present (R,S) and if double bond is present are cis/trans. In order to name a double bond as cis/trans, the important condition is that, an identical group has to be present on either side of the double bond. If the identical groups are present on the same side of double bond, then it is known as cis. If the identical groups are present on the opposite side of the double bond then it is known as trans.
The groups that are connected to the main carbon chain is known as substituents. The substituents are identified after the carbon chain is identified and the functional group present in the given compound also identified. The substituents are named by adding “yl” to the end of the name which indicate that it is a substituent is an alkyl. The
The longest carbon chain is known as the parent. Parent carbon chain is the lengthiest carbon chain in the molecule that must include the functional group that is present in the compound. The longest carbon chain is identified and the parent name is given by the number of carbon atoms that is present in it. It must be remembered that even though functional group is not present in parent carbon chain, the double bond, triple bond if present has to be included. Numbering becomes a part of all the parts in IUPAC name. After identifying the parent chain, the numbering is done. If functional group is present in the given compound, the numbering is given in such a way that the functional group gets the least number. Then the double bond, triple bond.
Number of carbon atoms in chain | Parent |
1 | Meth |
2 | Eth |
3 | Prop |
4 | But |
5 | Pent |
6 | Hex |
Unsaturation indicates that if any triple or double bonds are present in the molecule. If a compound contains a double bond it is named as “-en-” and if a triple bond is present “-yn-” is used. If a compound contains two double bonds, then it is named as “-dien-”. If three double bonds are present in the given compound, then it is named as “-trien-”. This same rule applies for the compound that contains multiple triple bonds also.
Functional group is the one after which the considered compound is being named.
Functional Group | Class of compound | Suffix |
![]() | Ester | -oate |
![]() | Ketone | -one |
![]() | Aldehyde | -al |
![]() | -oic acid | |
![]() | Alcohol | -ol |
![]() | -amine |

Want to see the full answer?
Check out a sample textbook solution
Chapter 5 Solutions
Organic Chemistry As a Second Language: First Semester Topics
- Indicate whether the product of the reaction between Naphthalene and CrO3 in acetic acid at 25ºC is 1,4 naphthoquinone or phthalic anhydride.arrow_forwardIndicate the products of the reaction between CH3COCH2COOC2H5 and Na+-OC2H5.arrow_forwardPrimary, Secondary, and Tertiary Alcohols O-H O-H O-H R₁-C-H R₁-C-H R₁-C-R₁ H R₂ R₂ Primary Alcohol Secondary Alcohol ChemistryLearner.com R stands for Carbon group like ethyl methyl propyl Tertiary Alcohol If 1 carbon group with two H attached to alcoholic carbon, then primary If 2 carbon group and 1 H are attached to alcoholic carbon, then secondary IF 3 carbon group and no H attach to alcoholic carbon then tertiary. The bottom line Starting "Weak" oxidant material PCC, DMP, Swern, etc Primary alcohol Aldehyde OH Secondary alcohol Ketone OH "Strong" oxidant KMnO4, H₂CrO4 (or equivalent) OH Carboxylic acid 요 Ketone No reaction No reaction Tertiary alcohol 1. Is ethanol a primary, secondary, or tertiary alcohol? Write out the structures of ethanol and any oxidation products of ethanol. If there is more than one oxidation product, give the structure of each of the products. 2. Is 2-propanol a primary, secondary, or tertiary alcohol? Write out the structures of 2-propanol and any…arrow_forward
- Complete the following equations hand written pleasearrow_forwardComplete the following equations please hand written pleasearrow_forwardUsing the Nernst equation to calculate nonstandard cell voltage A galvanic cell at a temperature of 25.0 °C is powered by the following redox reaction: 3+ 3Cu²+ (aq) +2Al(s) → 3 Cu(s)+2A1³* (aq) 2+ Suppose the cell is prepared with 5.29 M Cu in one half-cell and 2.49 M A1³+ in the other. Calculate the cell voltage under these conditions. Round your answer to 3 significant digits. x10 μ ☑ 00. 18 Ar Иarrow_forward
- Please help me solve this homework problemarrow_forwardPlease help me answer this homework questionarrow_forwardCalculating standard reaction free energy from standard reduction... Using standard reduction potentials from the ALEKS Data tab, calculate the standard reaction free energy AG° for the following redox reaction. Be sure your answer has the correct number of significant digits. 3+ H2(g)+2OH¯ (aq) + 2Fe³+ (aq) → 2H₂O (1)+2Fe²+ (aq) 0 kJ x10 Х ? olo 18 Ararrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY





