- Chapter 1: Introduction
- Chapter 10: Atomic Emission Spectrometry
- Chapter 11: AtomicMass Spectrometry
- Chapter 12: Atomic X-ray .Spectrometry
- Chapter 13: An Introduction to Ultraviolet-Visible Molecular Absorption Spectrometry
- Chapter 14: Applications of Ultraviolet -Visible Molecular Absorption SpectrQmetry
- Chapter 15: Molecular Luminescence Spectrometry
- Chapter 16: An Introduction to Infrared Spectrometry
- Chapter 17: Applications of Infrared Spectrometry
- Chapter 18: Raman Spectroscopy
- Chapter 19: Nuclear Magnetic Resonance Spectroscopy
- Chapter 2: Electrical Components and Circuits
- Chapter 20: Molecular Mass Spectrometry
- Chapter 21: Surface Characterization by Spectroscopy and Microscopy
- Chapter 22: An Introduction to Electroanalytical Chemistry
- Chapter 23: Potentiometry
- Chapter 24: Coulometry
- Chapter 25: Voltammetry
- Chapter 26: An Introduction to Chromatographic Separations
- Chapter 27: Gas Chromatography
- Chapter 28: Liquid Chromatography
- Chapter 29: Supercritical Fluid ChromatograpJty and Extraction
- Chapter 3: Operational Amplifiers in Chemical Instrumentation
- Chapter 30: Capillary Electrophorosis, Capillar Electrochromatography and Field-Flow Fractionation
- Chapter 31: Thermal Methods
- Chapter 32: Radiochemical Methods
- Chapter 33: Automated Methods of Analysis
- Chapter 34: Particle Size Determination
- Chapter 4: Digital Electronics and Computers
- Chapter 5: Signals and Noise
- Chapter 6: An Introduction to Spectrometric Methods
- Chapter 7: Components of Optical Instruments
- Chapter 8: An Introduction to Optical Atomic .Spectrometry
- Chapter 9: Atomic Absorption and Atomic Fluorescence Spectrometry
Principles of Instrumental Analysis 6th Edition - Solutions by Chapter
Full solutions for Principles of Instrumental Analysis | 6th Edition
Compounds containing a carbon-carbon triple bond.
An organic compound that has an NR2 group attached to a carbonyl. (Section 24.4)
A compound containing an sp3 -hybridized nitrogen atom bonded to one, two, or three carbon atoms
Compounds consisting of a single ring containing a fully conjugated p system. Benzene is annulene.
Carbonyl group (Section 1.3C)
A C"O group.
Properties of solutions that depend on the number of solute particles in solution and not on the nature of the solute particles. (12.6)
A measure of a solvent’s ability to insulate opposite charges from one another
A compound containing two hydroxyl groups (OH).
A reaction in which the reaction rate is proportional to the concentration of a single reactant, raised to the first power. (Section 14.4)
The energy released when 1 g of a substance is combusted. (Section 5.8)
A method forpreparing primary amines that avoids formation of secondary and tertiary amines.
A carbohydrate in which the !OH on its anomeric carbon is replaced by !OR
A polymer in which the repeating units contain chirality centers which all have the same configuration.
The nucleophile in a Michael reaction.
In NMR spectroscopy, a technique in which only the one-bond couplings are observed. CH3 groups appear as quartets, CH2 groups appear as triplets, CH groups appear as doublets, and quaternary carbon atoms appear as singlets.
Possessing radioactivity, the spontaneous disintegration of an unstable atomic nucleus with accompanying emission of radiation. (Section 2.2; Chapter 21: Introduction)
sigma 1S2 bond
A covalent bond in which electron density is concentrated along the internuclear axis. (Section 9.6)
Atomic orbitals that are achieved by mathematically averaging one s orbital with two p orbitals to form three hybridized atomic orbitals.
The distance between adjacent peaks of an oscillating magnetic or electric field.
A method for converting a carbonyl group into a methylene group (CH2) under basic conditions.