
Concept explainers
Interpretation: The systematic name of the unbranched
Concept introduction:
Systematic Name: It is a standardized name given for a chemical compound in systematic manner. Any organic molecule can be named by using IUPAC (International Union for Pure and applied chemistry) rules. IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule. It can be any alkyl group and carboxy, amino, cyano etc…
Suffix represents the substituent present in the molecule. It can be any
Root word represents the longest continuous carbon skeleton present in the organic molecule.
When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo.
IUPAC naming for Alkane:
Name the main chain: Find the longest carbon chain and name the chain according to the number of carbon atoms it contains; is also the suffix part of the name.
Number the carbon atoms in the main chain: The carbons are numbered, in which the substituents must get lowest possible numbers.
Identify the substituents, and number each: The number at where substituents are present has to be noted. The substituents written as prefix.
Write the names as a single word: Use the hyphen to separate the numbers from the different prefix; commas to separate numbers. If two or more different substituents are present, arrange them in alphabetical order. If two or more identical substituents are present, use prefixes di-, tri-, tetra-, but this particular prefix should not be used for alphabetizing purpose.

Answer to Problem 1PS
The systematic name of the given alkane
Explanation of Solution
The molecular formula of alkane is given. The longest chain has seven carbon atoms so parent chain will be
Therefore systematic name of the given alkane
Want to see more full solutions like this?
Chapter 23 Solutions
Bundle: Chemistry & Chemical Reactivity, Loose-Leaf Version, 9th + OWLv2, 4 terms (24 Months) Printed Access Card
- ASP please....arrow_forwardNonearrow_forwardConsider the structure of 1-bromo-2-fluoroethane. Part 1 of 2 Draw the Newman projection for the anti conformation of 1-bromo-2-fluoroethane, viewed down the C1-C2 bond. ✡ ぬ Part 2 of 2 H H F Br H H ☑ Draw the Newman projection for the gauche conformation of 1-bromo-2-fluoroethane, viewed down the C1-C2 bond. H F Br H Harrow_forward
- Please help me answer this question. I don't understand how or where the different reagents will attach and it's mostly due to the wedge bond because I haven't seen a problem like this before. Please provide a detailed explanation and a drawing showing how it can happen and what the final product will look like.arrow_forwardWhich of the following compounds is the most acidic in the gas phase? Group of answer choices H2O SiH4 HBr H2Sarrow_forwardWhich of the following is the most acidic transition metal cation? Group of answer choices Fe3+ Sc3+ Mn4+ Zn2+arrow_forward
- Based on the thermodynamics of acetic acid dissociation discussed in Lecture 2-5, what can you conclude about the standard enthalpy change (ΔHo) of acid dissociation for HCl? Group of answer choices You cannot arrive at any of the other three conclusions It is a positive value It is more negative than −0.4 kJ/mol It equals −0.4 kJ/molarrow_forwardPLEASE HELP URGENT!arrow_forwardDraw the skeletal structure corresponding to the following IUPAC name: 7-isopropyl-3-methyldecanearrow_forward
- Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
- Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub CoChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning



