
Concept explainers
Write a balanced chemical equation for the combustion of each of the following compounds:
a) Decane
b) Cyclodecane
c) Methylcyclononane
d) Cyclopentylcyclopentane

Interpretation:
A balanced chemical equation for the combustion of each of the given compounds is to be written.
Concept introduction:
Alkanes are inert in acid-base reactions but undergo oxidation-reduction reactions.
During combustion, alkanes undergo oxidation.
This combustion reaction of alkanes is exothermic, and the products formed are carbon dioxide and water.
When balancing the reaction, the carbon and hydrogen is balanced first, leaving oxygen for the last to balance.
Answer to Problem 39P
Solution:
a)
b)
c)
d)
Explanation of Solution
a) Decane
Decane is a straight chain alkane having the molecular formula
The combustion reaction of decane is written as follows:
To balance this reaction, first, the C and H are balanced.
Oxygen is balanced as follows:
The coefficients are converted to whole numbers as follows:
This is the complete balanced reaction of decane.
b) Cyclodecane
Cyclodecane is a cyclic alkane having the molecular formula
The combustion reaction of cyclodecane is written as follows:
To balance this reaction, first, the C and H are balanced.
Oxygen is balanced as follows:
This is the complete balanced reaction of cyclodecane.
c) Methylcyclononane
Methylcyclononane is a branched chain alkane having the molecular formula
The combustion reaction of methylcyclononane is written as follows:
To balance this reaction, first, the C and H are balanced.
Oxygen is balanced as follows:
This is the complete balanced reaction of methylcyclononane.
d) Cyclopentylcyclopentane
Cyclopentylcyclopentane is a branched chain alkane having the molecular formula
The combustion reaction of Cyclopentylcyclopentane is written as follows:
To balance this reaction, first, the C and H balanced.
Oxygen is balanced as follows:
The coefficients are converted to whole numbers as follows:
This is the complete balanced reaction of cyclopentylcyclopentane.
Want to see more full solutions like this?
Chapter 2 Solutions
Organic Chemistry - Standalone book
- Question 3 Shown below are the absorption and emission spectra of anthracene at room temperature. Absorbance or fluorescence intensity Absorption Fluorescence 300 340 380 Absorption max. 375 nm Anthracene Fluorescence max. 397 nm Tfl 6 ns Φε 0.36 420 460 Wavelength (nm) (a) Explain why anthracene fluorescence occurs at a longer wavelength than does absorption. (b) The emission and absorption spectra are mirror images. Why is this so? (c) What changes would you expect to see if these spectra were measured at 77 K? Explain your answer. (d) Anthracene fluorescence does not show solvatochromism. What is solvatochromism and what does its absence indicate about the electronic structure of anthracene? (e) At 77 K, anthracene shows a weak phosphorescence at 680 nm. (i) Draw a Jablonski diagram for anthracene. (ii) Explain why this peak at 680 nm is absent at room temperature. (iii) What would happen to this emission if anthracene was substituted with iodine (i.e. iodoanthracene)?arrow_forwardWhat is oxygenarrow_forwardWhat is the predicted product when estradiol is treated with excess NaH followed by excess bromopropane? OH HO HO Ilm H www I Ι H Iw excess 1. NaH 2. bromopropanearrow_forward
- Choose a Haworth projection for the following compounds: a-D-Mannopyranose OH OH OH OH ° OH ㅎ. OH OH OH OH OH OH OH OH OH OHarrow_forwardChoose a Haworth projection for the following compounds: B-D-Galactopyranose: OH OH OH OH OH OH OH OH OH OH OH OH OH OH OHarrow_forwardConsider the structure of the following cyclic octapeptide. Would cleavage of this peptide with trypsin produce different fragments than cleavage with chymotrypsin? Explain. Phe Arg Arg Phe Phe Arg Phe Arg Cleavage with trypsin will produce Arg-Phe, while cleavage with chymotrypsin will produce Phe-Arg. These dipeptides are not the same. They are constitutional isomers. ○ Cleavage with trypsin will produce Phe-Arg, while cleavage with chymotrypsin will produce Arg-Phe. These dipeptides are not the same. They are constitutional isomers. Cleavage with trypsin will produce Arg-Phe, while cleavage with chymotrypsin will produce Phe-Arg. These dipeptides are the same. ○ Cleavage with trypsin will produce Phe-Arg, while cleavage with chymotrypsin will produce Arg-Phe. These dipeptides are the same.arrow_forward
- Which of the given compounds is a phosphatidic acid? CH2OC(CH2)14CH3 СН2ОС(СН2)14 СН3 о CHOC(CH2)16CH 3 CHOC(CH2)16 CH3 СН2ОР(ОН)2 CH₂OC(CH2)14 CH3 CH₂OC(CH2)14CH3 CHOH СН2ОР(ОН)2 Ш || CH2OH CHOH СН2ОР(ОН)2 IVarrow_forwardWhich of the compounds shown would produce D-glucose and D-mannose when treated with HCN followed by H2/Pd/BaSO4/H₂O? H H H || ○ IV OV HO -H H -OH H- -OH HO -H HO- -H H- -OH H -OH HO -H HO -H H -OH HO -H H -OH HO -H H -OH H- -OH CH2OH | CH₂OH CH₂OH CH2OH CH₂OH || ||| IV Varrow_forwardWhich of the compounds shown would produce D-glucose and D-mannose when subjected to Kiliani-Fischer synthesis? H H H H 01 ○ II O IV OV HO- -H H- -OH H- -ОН НО H HỌ -H H- -OH H OH HO- -H HO -H H- -OH HO -H H- OH HO- -H H- OH H -OH CH2OH | CH2OH CH2OH CH2OH CH₂OH || ||| IV Varrow_forward
- Choose a Haworth projection for the following compounds: a-D-Glucopyranose . OH OH OH OH OH OH OH OH OH OH OH OH OH - OH OHarrow_forwardIdentify the expected major product of the following reaction. O। ○ II III IV OV || Cl2 hv ||| IV CIarrow_forwardIdentify the expected major product of the following reaction. ΟΙ || IV x excess H2, Ni 100 atm 150°C ? HO. G G G G || III IVarrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co



