- 2.2-1: Fur d" ...t'Tllhling lhe \'l)ILlgL' di\idcr "ih()wl1 bclnw.l\\'(l o...
- 2.2-2: Assume that for a circuit similar to that shown in 2\. R, = 20011.R...
- 2.2-3: For a circuit similar to the one shown in 2-\, RI ~ 1.00 Ul, R, = 2...
- 2.2-4: A voltmeter was used to measure the voltage of a cell with an inter...
- 2.2-5: For the following circuit, calculate .(a) the potential difference ...
- 2.2-6: For the circuit shown helow. calculatefa) the power dissipated betw...
- 2.2-7: Thle circuit that follows is for a laboratory potentiometer for mea...
- 2.2-8: Show that the data in the last column of Table 2-1 arc correct.
- 2.2-9: Show that the data in the last column of Tahle 2-2 are correct.
- 2.2-10: The current in a circuit is to he determined by measuring the volta...
- 2.2-11: An electrolysis at a nearlv t'. , cons ant current can he performed...
- 2.2-12: Repeat the calculations in II. assuming that \'H = 9.1l V andR = 0....
- 2.2-13: A 24- V de voltage source was connected in series with a resistor a...
- 2.2-14: How long would it take to discharge a 0.0 IS flF capacitor to I % o...
- 2.2-15: Calculate time constants for each of the RC circuits described in P...
- 2.2-16: A series RC circuit consists of a 25- V dc source. a 50 kll resisto...
- 2.2-17: Repeat the calculations in 2-16. assuming that the voltage source w...
- 2.2-18: Calculate the capacitive reactance, the impedance. and the phase an...
- 2.2-19: Derive a frequency response curve for a low-pass RC filter in which...
- 2.2-20: Derive a frequency response cur\'e for a high-pass RC tilter in whi...
- 2.2-21: The circuit shown hel,)\\' is a network of lour capacitors connecte...
Solutions for Chapter 2: Electrical Components and Circuits
Full solutions for Principles of Instrumental Analysis | 6th Edition
The resonancestabilized, cationic intermediate of a Friedel-Crafts acylation, formed by treating an acyl halide with aluminum trichloride.
Members of group 1A in the periodic table. (Section 7.7)
alpha (a) anomer
The cyclic hemiacetal of an aldose in which the hydroxyl group at the anomeric position is trans to the CH2OH
A conformation about a single bond in which two groups on adjacent carbons lie at a dihedral angle of 180°.
Atoms that lie in the same plane.
Having the same energy.
The spreading of electron density over a larger volume of space.
A molecule composed of only two atoms. (Section 2.6)
The branch of chemistry that deals with the relationships between electricity and chemical reactions. (Chapter 20: Introduction)
Any process with a negative DH (the system gives energy to the surroundings).
A compound containing a halogen atom and a hydroxyl group on adjacent carbons; those containing Br and OH are bromohydrins, and those containing Cl and OH are chlorohydrins.
A bond that results from the force of attraction between two oppositely charged ions.
A carbohydrate for which the chirality center farthest from the carbonyl group will have an OH group pointing to the left in the Fischer projection.
The change in specifi c rotation that occurs when an a or b hemiacetal form of a carbohydrate in aqueous solution is converted to an equilibrium mixture of the two forms.
An ion in which oxygen bears a positive charge.
The special name given to the amide bond formed between the a-amino group of one amino acid and the a-carboxyl group of another amino acid
pH titration curve
A graph of pH as a function of added titrant. (Section 17.3)
Plane of symmetry
An imaginary plane passing through an object dividing it so that one half is the mirror image of the other half
A test for determining the relationship between two protons. The compound is drawn two times, each time replacing one of the protons with deuterium. If the two compounds are identical, the protons are homotopic. If the two compounds are enantiomers, the protons are enantiotopic. If the two compounds are diastereomers, the protons are diastereotopic.
The carbon atoms of a carbon-carbon double bond.