CHEMISTRY-W/MASTERING CHEMISTRY ACCESS
8th Edition
ISBN: 9780135205068
Author: Robinson
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 23, Problem 23.81SP
Interpretation Introduction
Interpretation:
The line drawing of a cyclic molecule with six carbon atoms and a cis double bond is to be drawn and the reason of unavailability of a trans- double bond is to be discussed.
Concept introduction:
The line drawing is chemical structure in which carbon and hydrogen molecules are not drawn, in these types of structure lines are used to draw structure representing molecules.
The cis- double bond is when two groups attached to the carbons of the double bond are on the same side of the double bond and the trans- double bond is when two groups attached to the carbons of the double bond are on the different sides of the double bond.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
The heat of combustion of decahydronaphthalene(C10H18) is -6286 kJ/mol. The heat of combustion ofnaphthalene (C10H8) is -5157 kJ/mol. (In both casesCO2(g) and H2O(l) are the products.) Calculate the heat of hydrogenationand the resonance energy of naphthalene.
Isotretinoin is a retinoid derivative of vitamin A used in the treatment of severe recalcitrant acne. What is the degree of substitution
of the encircled alkene functional group in its structure?
...
А
tetrasubstituted
B) trisubstituted
c) monosubstituted
D
disubstituted
22:25
Worksheet 2 chemistry
Worksheet 2: Formulae and structures of organic compounds
Complete the table below to identify the general formulae and structures of the organic compounds. Give reasons why.
Name
Homologous series
Structural formula
General formula
(homologous series)
Propan-1-ol
Alcohol
Reasons
Propan-2-ol
Reasons
2-methypropan-2-ol
Worksheet 2: Formulae and structures of organic compounds
Reasons
2-Bromopropane
Reasons
Propanone
Reasons
| 1-Propanal
Reasons
ج ال..
Chapter 23 Solutions
CHEMISTRY-W/MASTERING CHEMISTRY ACCESS
Ch. 23 - Prob. 23.1PCh. 23 - Prob. 23.2ACh. 23 - Prob. 23.3PCh. 23 - Prob. 23.4ACh. 23 - Prob. 23.5PCh. 23 - Prob. 23.6ACh. 23 - Draw a complete electron-dot structure for...Ch. 23 - Limonene is the major component in the oil of...Ch. 23 - Draw an orbital overlap picture for methyl a mine...Ch. 23 - Prob. 23.10A
Ch. 23 - Draw an orbital overlap picture for formaldehyde,...Ch. 23 - Prob. 23.12ACh. 23 - Prob. 23.13PCh. 23 - Prob. 23.14ACh. 23 - Prob. 23.15PCh. 23 - Draw complete electron-dot structures from the...Ch. 23 - Prob. 23.17PCh. 23 - Prob. 23.18ACh. 23 - Draw a simplified orbital overlap picture of...Ch. 23 - Prob. 23.20ACh. 23 - Prob. 23.21PCh. 23 - Prob. 23.22ACh. 23 - Prob. 23.23PCh. 23 - Prob. 23.24ACh. 23 - Prob. 23.25PCh. 23 - Prob. 23.26ACh. 23 - Asparagine is a naturally occurring aminoacid that...Ch. 23 - Prob. 23.28PCh. 23 - Prob. 23.29PCh. 23 - Prob. 23.30CPCh. 23 - Prob. 23.31CPCh. 23 - Prob. 23.32CPCh. 23 - Prob. 23.33CPCh. 23 - Prob. 23.34CPCh. 23 - Prob. 23.35CPCh. 23 - The following structure is a representation of...Ch. 23 - Prob. 23.37CPCh. 23 - Prob. 23.38CPCh. 23 - Prob. 23.39CPCh. 23 - Prob. 23.40SPCh. 23 - Prob. 23.41SPCh. 23 - Draw a straight-chain alkane with 6 carbon atoms...Ch. 23 - Prob. 23.43SPCh. 23 - Prob. 23.44SPCh. 23 - Prob. 23.45SPCh. 23 - The following line drawings represent two amino...Ch. 23 - Prob. 23.47SPCh. 23 - Prob. 23.48SPCh. 23 - Prob. 23.49SPCh. 23 - Prob. 23.50SPCh. 23 - Prob. 23.51SPCh. 23 - Prob. 23.52SPCh. 23 - Prob. 23.53SPCh. 23 - Prob. 23.54SPCh. 23 - Prob. 23.55SPCh. 23 - Prob. 23.56SPCh. 23 - Prob. 23.57SPCh. 23 - Prob. 23.58SPCh. 23 - Give a line drawing and molecular formula for the...Ch. 23 - Prob. 23.60SPCh. 23 - Prob. 23.61SPCh. 23 - Prob. 23.62SPCh. 23 - Prob. 23.63SPCh. 23 - Prob. 23.64SPCh. 23 - Prob. 23.65SPCh. 23 - Draw the complete electron-dot structure and...Ch. 23 - Prob. 23.67SPCh. 23 - Prob. 23.68SPCh. 23 - Prob. 23.69SPCh. 23 - Prob. 23.70SPCh. 23 - Prob. 23.71SPCh. 23 - Prob. 23.72SPCh. 23 - Prob. 23.73SPCh. 23 - Prob. 23.74SPCh. 23 - Prob. 23.75SPCh. 23 - Prob. 23.76SPCh. 23 - Prob. 23.77SPCh. 23 - Prob. 23.78SPCh. 23 - Prob. 23.79SPCh. 23 - Prob. 23.80SPCh. 23 - Prob. 23.81SPCh. 23 - Prob. 23.82SPCh. 23 - Prob. 23.83SPCh. 23 - Prob. 23.84SPCh. 23 - Prob. 23.85SPCh. 23 - Prob. 23.86SPCh. 23 - What does it mean to say that fats and oils are...Ch. 23 - Prob. 23.88SPCh. 23 - Prob. 23.89SPCh. 23 - Prob. 23.90SPCh. 23 - Prob. 23.91SPCh. 23 - Prob. 23.92SPCh. 23 - Prob. 23.93SPCh. 23 - Prob. 23.94SPCh. 23 - Prob. 23.95SPCh. 23 - Prob. 23.96SPCh. 23 - Prob. 23.97SPCh. 23 - Prob. 23.98SPCh. 23 - Prob. 23.99SPCh. 23 - Prob. 23.100SPCh. 23 - Prob. 23.101SPCh. 23 - Prob. 23.102SPCh. 23 - Prob. 23.103SPCh. 23 - Prob. 23.104SPCh. 23 - Prob. 23.105SPCh. 23 - Prob. 23.106SPCh. 23 - Prob. 23.107SPCh. 23 - Prob. 23.108SPCh. 23 - Prob. 23.109SPCh. 23 - Prob. 23.110SPCh. 23 - Prob. 23.111SPCh. 23 - Prob. 23.112SPCh. 23 - Prob. 23.113SPCh. 23 - What amino acids do the following abbreviations...Ch. 23 - Name and draw the structures of amino acids that...Ch. 23 - Identify the amino acids present in the following...Ch. 23 - Prob. 23.117SPCh. 23 - Prob. 23.118SPCh. 23 - Prob. 23.119SPCh. 23 - Prob. 23.120SPCh. 23 - Prob. 23.121SPCh. 23 - Prob. 23.122SPCh. 23 - Prob. 23.123SPCh. 23 - Prob. 23.124SPCh. 23 - Prob. 23.125SPCh. 23 - Prob. 23.126SPCh. 23 - Prob. 23.127SPCh. 23 - Prob. 23.128SPCh. 23 - Prob. 23.129SPCh. 23 - Prob. 23.130SPCh. 23 - Prob. 23.131SPCh. 23 - Prob. 23.132SPCh. 23 - Prob. 23.133SPCh. 23 - Prob. 23.134MPCh. 23 - Prob. 23.135MPCh. 23 - Cytochrome c is an important enzyme found in the...Ch. 23 - Prob. 23.137MPCh. 23 - Prob. 23.138MP
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
- H H Write the structures of the alkenes that would yield the following carbonyl compounds PRACTICE PROBLEM 8.22 when treated with ozone and then with dimethyl sulfide. (a) and (c) EO and `H oalio (2 mol is produced from 1 mol of alkene) (b) H.arrow_forwardSome of the following examples can show geometric isomerism, and some cannot. Forthe ones that can, draw all the geometric isomers, and assign complete names using theE-Z system.(a) 3-bromo-2-chloropent-2-enearrow_forwardWhich of (a)-(d) is not aromatic? (B) (A) (C) (D)arrow_forward
- (a) Which compounds (B–F) are identical to A? (b) Which compounds (B–F) represent an isomer of A?arrow_forwardCompound X has the formula C35H54BR2. When X is treated with excess H2 over Pd/C, the product has the formula C35H66Br2. How many double bonds are in X?arrow_forwardLipoic acid is required by many microorganisms for proper growth. As a disulfide, it functions in the living system by catalyzing certain oxidation reactions and is reduced in the process. Write the structure of the reduction product.arrow_forward
- Biphenyl has the following structure.(a) Is biphenyl a (fused) polynuclear aromatic hydrocarbon?(b) How many pi electrons are there in the two aromatic rings of biphenyl? How does this number compare with that for naphthalene?arrow_forwardDraw the structures of the following compounds. (a) isobutyl bromidearrow_forwardWhich is least reactive in electrophilic aromatic substitution? (A) (B) CH3 (C) CHO (D) C3arrow_forward
- Both alkenes and alkynes under hydrogenation by the same reaction mechanism. Draw the line angle formula for chalcone. How many nonaromatic pi bonds does it have? Is it an alkene or an alkyne? Aromatic pi bonds are much more resist to chemical reactions than those of alkenes or alkynes, and will not react in ordinary alkene and alkyne reactions. Given that, draw the structure of the product you expect to be formed. Will the addition of hydrogen be syn or anti? Only second part of question draw structure of productarrow_forwardWhat is the main difference between an aromatic and an anti-aromatic compound? O None of these O Aromatic compounds must satisfy Hückel's rule. O Anti-aromatic compounds must have a conjugated system with a p orbital at every vertex. O Aromatic compounds must be cyclic and planar but not anti-aromatic compounds. O Aromatic compounds must be monocyclic.arrow_forwardThe IUPAC name of the compound H- is (a) 5-formylhex-2-en-3-one (b) 5-methyl-4-oxohex-2-en-5-al (c) 3-keto-2-methylhex-5-enal (d) 3-keto-2-methylhex-4-enal ( The correct statement regarding electrophile is (a) electrophile is a negatively charged species and can form a bond by accepting a pair of electrons from another electrophile (b) electrophiles are generally neutral species and can form a bond by accepting a pair of electrons from a nucleophile (c) electrophile can be either neutral or ar positively charged species and can form a bond by accepting a pair of electrons from a nucleophile (d) electrophile is a negatively charged species and can form a bond by accepting a pair of electrons from a nucleophile.. Which among the given molecules can exhibit tautomerism? Ph Ph I II III (a) III only (c) Both I and II (b) Both I and III (d) Both II and III 1) Which of the following biphenyls is optically active?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
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