- 3.16.55: Draw a condensed structure and a skeletal structure for each of the...
- 3.16.56: List the following compounds from highest boiling to lowest boiling:
- 3.16.57: a. What is each compounds systematic name?b. Draw a skeletal struct...
- 3.16.58: Which of the following represents a cis isomer?
- 3.16.59: a. How many primary carbons does each of the following compounds ha...
- 3.16.60: Which of the following conformers of isobutyl chloride is the most ...
- 3.16.61: Draw a skeletal structure for an alkane that hasa. six carbons, all...
- 3.16.62: What is each compounds systematic name?a. CH3CH2CHCH3NH2e. CH3CHCH2...
- 3.16.63: Which hasa. the higher boiling point: 1-bromopentane or 1-bromohexa...
- 3.16.64: a. Draw Newman projections of the two conformers of cis-1,3-dimethy...
- 3.16.65: Ansaid and Motrin belong to the group of drugs known as nonsteroida...
- 3.16.66: Draw a picture of the hydrogen bonding in methanol.
- 3.16.67: A student was given the structural formulas of several compounds an...
- 3.16.68: Which of the following conformers has the highest energy (is the le...
- 3.16.69: Give the systematic names for all alkanes with molecular formula C7...
- 3.16.70: Draw skeletal structures for the following:a. 5-ethyl-2-methyloctan...
- 3.16.71: For rotation about the C@3 C@4 bond of 2-methylhexane, do the follo...
- 3.16.72: Draw all the isomers that have molecular formula C5H11Br. (Hint: Th...
- 3.16.73: What is each compounds systematic name?
- 3.16.74: Draw the two chair conformers for each of the following and indicat...
- 3.16.75: Why are lower molecular weight alcohols more soluble in water than ...
- 3.16.76: a. Draw a potential energy diagram for rotation about the CC bond o...
- 3.16.77: For each of the following compounds, determine whether the cis isom...
- 3.16.78: How many ethers have molecular formula C5H12O? Draw their structure...
- 3.16.79: Draw the most stable conformer of the following molecule. (A solid ...
- 3.16.80: What is each compounds systematic name?
- 3.16.81: Calculate the energy difference between the two chair conformers of...
- 3.16.82: The most stable form of glucose (blood sugar) is a six-membered rin...
- 3.16.83: What is each compounds systematic name?
- 3.16.84: Explain the following:a. 1-Hexanol has a higher boiling point than ...
- 3.16.85: One of the chair conformers of cis-1,3-dimethylcyclohexane is 5.4 k...
- 3.16.86: Bromine is a larger atom than chlorine, but the equilibrium constan...
- 3.16.87: Name the following compounds:
- 3.16.88: Using the data obtained in 81, calculate the percentage of molecule...
- 3.16.89: Using the data obtained in 85, calculate the amount of steric strai...
Solutions for Chapter 3.16: Fused Cyclohexane Rings
Full solutions for Organic Chemistry | 8th Edition
A quantitative measure of the extent to which a compound absorbs radiation of a particular wavelength. A 5 log (I0/I ) where I0 is the incident radiation and I is the transmitted radiation
A summary of the results of many possible displacement reactions. (4.4)
The term describing a carbonyl group (CRO bond) connected to an alkyl group or aryl group.
The product formed when the !CHO group of an aldose is oxidized to a !COOH group
A carbohydrate that contains an aldehyde group.
A class of colored compounds that are formed via azo coupling.
The electronic structure of a solid, defining the allowed ranges of energy for electrons in a solid. (Section 12.7)
A copolymer in which the different homopolymer subunits are connected together in one chain.
A state in which the rates of the forward and reverse reactions are equal. (14.1)
Compounds that have the same molecular formula but differ in the way the atoms are connected.
Diastereomers that differ from each other in the configuration of only one chirality center.
lambda max (lmax)
In UVVis spectroscopy, the wavelength of maximum absorption.
In a BaeyerVilliger oxidation, the migration rates of different groups, which determine the regiochemical outcome of the reaction.
Nucleophilic aromatic substitution
A reaction in which a nucleophile, most commonly a halogen, on an aromatic ring is replaced by another nucleophile.
A device that measures the rotation of plane-polarized light caused by optically active compounds.
A nuclear decay process where a positron, a particle with the same mass as an electron but with a positive charge, symbol 0+1e, or b+ is emitted from the nucleus. (Section 21.1)
A theory that many molecules and ions are best described as a hybrid of several Lewis structures
Secondary structure of nucleic acids
The ordered arrangement of nucleic acid strands
Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.
The threedimensional shape of a protein.