GENERAL ORGANIC+BIO...(LL)-W/MOD.ACCESS
3rd Edition
ISBN: 9780134466699
Author: FROST
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 4, Problem 1IA.10Q
Summary Introduction
To determine:
The explanation of how the number of hydrogen atoms was written after each carbon in the condensed structures.
Introduction:
In condensed structure formula, organic structures are written from left to right in one line and this structural formula is simple as it does not show any bonds or lone pairs of atoms and shows no connectivity of atoms in a molecule.
It shows the shorter way to draw a molecule and is more simplified than Lewis structure. It shows all atoms except the vertical bonds and some horizontal bonds.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Draw the virtual orbitals for the planar and pyramidal forms of CH3 and for the linear and bent forms of CH2
Q2: Draw the molecules based on the provided nomenclatures below:
(2R,3S)-2-chloro-3-methylpentane:
(2S, 2R)-2-hydroxyl-3,6-dimethylheptane:
Q3: Describes the relationship (identical, constitutional isomers, enantiomers or diastereomers)
of each pair of compounds below.
ག
H
CH3
OH
OH
CH3
H3C
OH
OH
OH
//////////
C
CH3
CH3
CH3
CH3
H3C
CH 3
C/III.....
Physics & Astronomy
www.physics.northweste
COOH
H
нош.....
H
2
OH
HO
CH3
HOOC
H
CH3
CH3
CH3
Br.
H
H
Br
and
H
H
H
H
Chapter 4 Solutions
GENERAL ORGANIC+BIO...(LL)-W/MOD.ACCESS
Ch. 4 - Prob. 4.1PPCh. 4 - Prob. 4.2PPCh. 4 - Prob. 4.3PPCh. 4 - Draw a skeletal structure for ethane, C2H6. Do you...Ch. 4 - Prob. 4.5PPCh. 4 - Prob. 4.6PPCh. 4 - Draw a Lewis structure for each of the following...Ch. 4 - Draw a Lewis structure for each of the following...Ch. 4 - Prob. 4.9PPCh. 4 - Prob. 4.10PP
Ch. 4 - Prob. 4.11PPCh. 4 - Prob. 4.12PPCh. 4 - Write the condensed structure for the...Ch. 4 - Write the condensed structure for the...Ch. 4 - Write the skeletal structure for the alkane shown:...Ch. 4 - Write the skeletal structure for the alkane shown:...Ch. 4 - Identify the family of hydrocarbon present in the...Ch. 4 - Identify the family of hydrocarbon present in the...Ch. 4 - Identify all the functional groups present in the...Ch. 4 - Prob. 4.20PPCh. 4 - The most prevalent fatty acid in coconut oil is...Ch. 4 - The most common fatty acid found in animals is...Ch. 4 - Draw the condensed structural formula for each of...Ch. 4 - Give the correct name for each of the following...Ch. 4 - Draw the skeletal structure for each of the...Ch. 4 - Prob. 4.26PPCh. 4 - Prob. 4.27PPCh. 4 - Prob. 4.28PPCh. 4 - Prob. 4.29PPCh. 4 - Prob. 4.30PPCh. 4 - Determine the relationship between each of the...Ch. 4 - Determine the relationship between each of the...Ch. 4 - Determine if each of the following cycloalkanes or...Ch. 4 - Determine it each of the following cycloalkanes or...Ch. 4 - Mark the chiral centers in the following...Ch. 4 - Mark the chiral centers in the following...Ch. 4 - Convert each of the Lewis structures shown into a...Ch. 4 - Convert each of the Lewis structures in Problem...Ch. 4 - Prob. 4.39APCh. 4 - Prob. 4.40APCh. 4 - Convert the skeletal structures shown to condensed...Ch. 4 - Convert the skeletal structures shown to condensed...Ch. 4 - Prob. 4.43APCh. 4 - Prob. 4.44APCh. 4 - Alkanes are also referred to as saturated...Ch. 4 - Are alkanes considered polar or nonpolar...Ch. 4 - Give the skeletal structure and name of the...Ch. 4 - Give the skeletal structure and name of the...Ch. 4 - Name the following straight-chain alkanes or...Ch. 4 - Name the following straight-chain alkanes or...Ch. 4 - Explain the structural difference between a...Ch. 4 - Prob. 4.52APCh. 4 - Identify all of the functional groups in each of...Ch. 4 - Identify all of the functional groups in each of...Ch. 4 - Prob. 4.55APCh. 4 - Prob. 4.56APCh. 4 - Prob. 4.57APCh. 4 - Draw skeletal structures for each of the following...Ch. 4 - Prob. 4.59APCh. 4 - Prob. 4.60APCh. 4 - Prob. 4.61APCh. 4 - Prob. 4.62APCh. 4 - Prob. 4.63APCh. 4 - Prob. 4.64APCh. 4 - Prob. 4.65APCh. 4 - Prob. 4.66APCh. 4 - How many structural isomers are possible for the...Ch. 4 - Prob. 4.68APCh. 4 - Prob. 4.69APCh. 4 - Prob. 4.70APCh. 4 - For each of the following compounds, indicate...Ch. 4 - Prob. 4.72APCh. 4 - Determine whether each of the following is the cis...Ch. 4 - Determine whether each of the following is the cis...Ch. 4 - Prob. 4.75APCh. 4 - Prob. 4.76APCh. 4 - Mark the chiral centers in the following...Ch. 4 - Mark the chiral centers in the following...Ch. 4 - Prob. 4.79APCh. 4 - Prob. 4.80APCh. 4 - Prob. 4.81CPCh. 4 - Prob. 4.82CPCh. 4 - Prob. 1IA.1QCh. 4 - Prob. 1IA.2QCh. 4 - Prob. 1IA.3QCh. 4 - Prob. 1IA.4QCh. 4 - Prob. 1IA.5QCh. 4 - Prob. 1IA.6QCh. 4 - Prob. 1IA.7QCh. 4 - Prob. 1IA.8QCh. 4 - Prob. 1IA.9QCh. 4 - Prob. 1IA.10QCh. 4 - Prob. 1IA.11QCh. 4 - Prob. 2IA.1QCh. 4 - Prob. 2IA.2QCh. 4 - Prob. 2IA.3QCh. 4 - Prob. 2IA.4QCh. 4 - Prob. 2IA.5QCh. 4 - What is the molecular shape (geometry) of the...Ch. 4 - Prob. 2IA.7QCh. 4 - Prob. 1ICCh. 4 - Prob. 2ICCh. 4 - Prob. 3ICCh. 4 - Prob. 4IC
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Q1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label each compound as chiral or achiral. OH HO CI Br H CI CI Br CI CI Xf x f g Br D OH Br Br H₂N R. IN Ill I -N S OMe D II H CO₂H 1/111 DuckDuckGarrow_forwardThese are synthesis questions. You need to show how the starting material can be converted into the product(s) shown. You may use any reactions we have learned. Show all the reagents you need. Show each molecule synthesized along the way and be sure to pay attention to the regiochemistry and stereochemistry preferences for each reaction. If a racemic molecule is made along the way, you need to draw both enantiomers and label the mixture as "racemic". All of the carbon atoms of the products must come from the starting material! ? H Harrow_forwardQ5: Draw every stereoisomer for 1-bromo-2-chloro-1,2-difluorocyclopentane. Clearly show stereochemistry by drawing the wedge-and-dashed bonds. Describe the relationship between each pair of the stereoisomers you have drawn.arrow_forward
- Classify each pair of molecules according to whether or not they can participate in hydrogen bonding with one another. Participate in hydrogen bonding CH3COCH3 and CH3COCH2CH3 H2O and (CH3CH2)2CO CH3COCH3 and CH₂ CHO Answer Bank Do not participate in hydrogen bonding CH3CH2OH and HCHO CH3COCH2CH3 and CH3OHarrow_forwardNonearrow_forwardQ4: Comparing (3S,4S)-3,4-dimethylhexane and (3R,4S)-3,4-dimethylhexane, which one is optically active? Briefly explain.arrow_forward
- Nonearrow_forwardNonearrow_forwardGiven the standard enthalpies of formation for the following substances, determine the reaction enthalpy for the following reaction. 4A (g) + 2B (g) → 2C (g) + 7D (g) AHrxn =?kJ Substance AH in kJ/mol A (g) - 20.42 B (g) + 32.18 C (g) - 72.51 D (g) - 17.87arrow_forward
- Determine ASran for Zn(s) + 2HCl(aq) = ZnCl2(aq) + H2(aq) given the following information: Standard Entropy Values of Various Substance Substance So (J/mol • K) 60.9 Zn(s) HCl(aq) 56.5 130.58 H2(g) Zn2+(aq) -106.5 55.10 CI (aq)arrow_forward3) Catalytic hydrogenation of the compound below produced the expected product. However, a byproduct with molecular formula C10H12O is also formed in small quantities. What is the by product?arrow_forwardWhat is the ΔHorxn of the reaction? NaOH(aq) + HCl(aq) → H2O(l) + NaCl(aq) ΔHorxn 1= ________ kJ/molarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Introductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Lipids - Fatty Acids, Triglycerides, Phospholipids, Terpenes, Waxes, Eicosanoids; Author: The Organic Chemistry Tutor;https://www.youtube.com/watch?v=7dmoH5dAvpY;License: Standard YouTube License, CC-BY