- 2.2.1: Do the line-angle formulas in each pair represent the same compound...
- 2.2.2: Draw line-angle formulas for the three constitutional isomers with ...
- 2.2.3: Write IUPAC names for these alkanes.
- 2.2.4: Combine the proper prefix, infix, and suffix and write the IUPAC na...
- 2.2.5: Write the molecular formula, IUPAC name, and common name for each c...
- 2.2.6: Write molecular formulas for each bicycloalkane, given its number o...
- 2.2.7: Following are the structural formulas and names of four bicycloalka...
- 2.2.8: For 1,2-dichloroethane:(a) Draw Newman projections for all eclipsed...
- 2.2.9: Following is a chair conformation of cyclohexane with the carbon at...
- 2.2.11: Draw a chair conformation of 1,4-dimethylcyclohexane in which one m...
- 2.2.12: Which cycloalkanes show cis,trans isomerism? For each that does, dr...
- 2.2.13: Following is a planar hexagon representation for one isomer of 1,2,...
- 2.2.14: Here is one cis,trans isomer of 3,5-dimethylcyclohexanol. Complete ...
- 2.2.15: Arrange the alkanes in each set in order of increasing boiling poin...
- 2.2.16: Write a line-angle formula for each condensed structural formula.
- 2.2.17: Write the molecular formula of each alkane.
- 2.2.18: Using parentheses and subscripts, provide an even more abbreviated ...
- 2.2.19: Which statements are true about constitutional isomers?(a) They hav...
- 2.2.21: an !OH (hydroxyl group, Section 1.3A). Which structural formulas re...
- 2.2.22: Each of the following compounds is an amine (Section 1.3B). Which s...
- 2.2.23: Each of the following compounds is either an aldehyde or a ketone (...
- 2.2.24: Draw structural formulas and write IUPAC names for the nine constit...
- 2.2.25: Draw structural formulas for all of the following.(a) Alcohols with...
- 2.2.26: Write IUPAC names for these alkanes and cycloalkanes.
- 2.2.27: Write structural formulas and line-angle formulas for the following...
- 2.2.28: Explain why each is an incorrect IUPAC name and write the correct I...
- 2.2.29: For each IUPAC name, draw the corresponding structural formula and ...
- 2.2.32: Torsional strain resulting from eclipsed C!H bonds is approximately...
- 2.2.33: How many different staggered conformations are there for 2-methylpr...
- 2.2.34: Consider 1-bromopropane, CH3CH2CH2Br.(a) Draw a Newman projection f...
- 2.2.35: Consider 1-bromo-2-methylpropane and draw the following.(a) The sta...
- 2.2.36: Trans-1,4-di-tert-butylcyclohexane exists in a normal chair conform...
- 2.2.37: From studies of the dipole moment of 1,2-dichloroethane in the gas ...
- 2.2.38: Draw structural formulas for the cis and trans isomers of hydrindan...
- 2.2.39: Following are the alternative chair conformations for trans-1,2-dim...
- 2.2.41: Is cis,trans isomerism possible in alkanes?
- 2.2.42: Draw structural formulas for the cis and trans isomers of 1,2-dimet...
- 2.2.43: Name and draw structural formulas for all cycloalkanes with molecul...
- 2.2.44: Using a planar pentagon representation for the cyclopentane ring, d...
- 2.2.45: Gibbs free energy differences between axial-substituted and equator...
- 2.2.46: When cyclohexane is substituted by an ethynyl group, !C#CH, the ene...
- 2.2.47: Calculate the difference in Gibbs free energy in kilojoules per mol...
- 2.2.48: Draw the alternative chair conformations for the cis and trans isom...
- 2.2.49: Use your answers from 2.48 to complete the table showing correlatio...
- 2.2.51: Draw alternative chair conformations for each substituted cyclohexa...
- 2.2.52: 1,2,3,4,5,6-Hexachlorocyclohexane shows cis,trans isomerism. At one...
- 2.2.53: In 2.24, you drew structural formulas for all isomeric alkanes with...
- 2.2.54: What generalization can you make about the densities of alkanes rel...
- 2.2.55: What unbranched alkane has about the same boiling point as water? (...
- 2.2.56: Complete and balance the following combustion reactions. Assume tha...
- 2.2.57: Following are heats of combustion per mole for methane, propane, an...
- 2.2.58: Following are structural formulas and heats of combustion of acetal...
- 2.2.59: Without consulting tables, arrange these compounds in order of decr...
- 2.2.61: Following are structural formulas for 1,4-dioxane and piperidine. 1...
- 2.2.62: Following is a planar hexagon representation of l-fucose, a sugar c...
- 2.2.63: stereorepresentation of glucose (we discuss the structure and chemi...
- 2.2.64: Following is the structural formula and a ball-and-stick model of c...
- 2.2.65: Following is the structural formula and a ball-and-stick model of c...
Solutions for Chapter 2: Constitutional Isomerism in Alkanes
Full solutions for Organic Chemistry | 7th Edition
ISBN: 9781133952848
Since 58 problems in chapter 2: Constitutional Isomerism in Alkanes have been answered, more than 56827 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 2: Constitutional Isomerism in Alkanes includes 58 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Organic Chemistry was written by and is associated to the ISBN: 9781133952848.
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addition reaction.
A reaction in which one molecule adds to another. (24.2)
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alpha particles.
See alpha rays.
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azo coupling
An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.
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beta particles
Energetic electrons emitted from the nucleus, symbol 0-1e or b-. (Section 21.1)
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degenerate
Having the same energy.
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Ester
A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.
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heat
The flow of energy from a body at higher temperature to one at lower temperature when they are placed in thermal contact. (Section 5.1)
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ionic compound
A compound composed of cations and anions. (Section 2.7)
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isomers
Compounds whose molecules have the same overall composition but different structures. (Sections 2.9 and 23.4)
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Ketose
A monosaccharide containing a ketone group.
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oxidation state
A method of electron book-keeping in which all bonds are treated as if they were purely ionic.
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Part per million (ppm)
Units used on NMR spectra to record chemical shift relative to the TMS standard.
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phospholipids
Esterlike derivatives of phosphoric acid.
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photon
The smallest increment (a quantum) of radiant energy; a photon of light with frequency n has an energy equal to hn. (Section 6.2)
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Quantum mechanics
The branch of science that studies the interaction of matter and radiation.
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salinity
A measure of the salt content of seawater, brine, or brackish water. It is equal to the mass in grams of dissolved salts present in 1 kg of seawater. (Section 18.3)
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saturated
A compound that contains no p bonds.
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Step-growth polymerization
A polymerization in which chain growth occurs in a stepwise manner between difunctional monomers as, for example, between adipic acid and hexamethylenediamine to form nylon 66. Also called condensation polymerization.
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steric number
The total of (single bonds + lone pairs) for an atom in a compound.
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strong activators
Groups that strongly activate an aromatic ring toward electrophilic aromatic substitution, thereby significantly enhancing the rate of the reaction.