- 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
Rainwater that has become excessively acidic because of absorption of pollutant oxides, notably SO3, produced by human activities. (Section 18.2)
An organic compound containing the hydroxyl group —OH. (24.4)
alpha (a) position
The position immediately adjacent to a functional group.
Aryl group (Ar -)
A group derived from an arene by removal of an H.
A temperature scale on which water freezes at 0° and boils at 100° at sea level. (Section 1.4)
continuous-wave (CW) spectrometer
An NMR spectrometer that holds the magnetic field constant and slowly sweeps through a range of rf frequencies, monitoring which frequencies are absorbed.
Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be lower than that for benzene.
An organic compound that has an OR group attached to a carbonyl; it is the product of a reaction between a carboxylic acid and an alcohol. (Section 24.4)
The joining of two light nuclei to form a more massive one. (Section 21.6)
High-density lipoprotein (HDL)
Plasma particles, density 1.06–1.21 g/mL, consisting of approximately 33% proteins, 30% cholesterol, 29% phospholipids, and 8% triglycerides.
An ion or molecule that coordinates to a metal atom or to a metal ion to form a complex. (Section 23.2)
When electromagnetic radiation is viewed as a particle, an individual packet of energy.
A large molecule of high molecular mass, formed by the joining together, or polymerization, of a large number of molecules of low molecular mass. The individual molecules forming the polymer are called monomers. (Sections 12.1 and 12.8)
A triglyceride having several carbon-carbon double bonds in the hydrocarbon chains of its three fatty acids.
The energy that an object possesses as a result of its composition or its position with respect to another object. (Section 5.1)
The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.
An addition or substitution reaction in which one of two or more possible products is formed in preference to all others that might be formed.
A conformation of a conjugated diene in which the disposition of the two p bonds with regard to the connecting single bond is cis-like (a dihedral angle of 0°).
A nucleophilic substitution in which the solvent is also the nucleophile
The study of the interaction between matter and electromagnetic radiation.