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The rst obvious question to arise is, how are these equivalent source voltages, currents, and resistances computed The next few sections illustrate the computation of these equivalent circuit parameters, mostly through examples A substantial number of Check Your Understanding exercises are also provided, with the following caution: The only way to master the computation of Th venin and Norton e equivalent circuits is by patient repetition Determination of Norton or Thevenin Equivalent Resistance The rst step in computing a Th venin or Norton equivalent circuit consists of e nding the equivalent resistance presented by the circuit at its terminals This is done by setting all sources in the circuit equal to zero and computing the effective resistance between terminals The voltage and current sources present in the circuit are set to zero by the same technique used with the principle of superposition: voltage sources are replaced by short circuits, current sources by open circuits To illustrate the procedure, consider the simple circuit of Figure 333; the objective is to compute the equivalent resistance the load RL sees at port a-b In order to compute the equivalent resistance, we remove the load resistance from the circuit and replace the voltage source, vS , by a short circuit At this point seen from the load terminals the circuit appears as shown in Figure 334 You can see that R1 and R2 are in parallel, since they are connected between the same two nodes If the total resistance between terminals a and b is denoted by RT , its value can be determined as follows: RT = R3 + R1 R2 (328)

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regional centromere The type of centromere found in higher eukaryotes that can accommodate several spindle microtubules regulator gene A gene primarily involved in control of the production of another gene s product reinitiation The initiation of translation by a ribosome that has just completed translation of a region of the messenger RNA upstream of the current point of initiation relative Darwinian tness See tness relaxed mutant A mutant that does not exhibit the stringent response under amino acid starvation release factors (RFl and RF2) Proteins in prokaryotes responsible for termination of translation and release of the newly synthesized polypeptide when a nonsense codon appears in the A site of the ribosome Replaced by eRF in eukaryotes repetitive DNA DNA made up of copies of the same nucleotide sequence replica-plating A technique to rapidly transfer microorganism colonies to numerous petri plates.

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An alternative way of viewing RT is depicted in Figure 335, where a hypothetical 1-A current source has been connected to the terminals a and b The voltage vx appearing across the a-b pair will then be numerically equal to RT (only because iS = 1 A!) With the 1-A source current owing in the circuit, it should be apparent that the source current encounters R3 as a resistor in series with the parallel combination of R1 and R2 , prior to completing the loop

Chattopadhyay, A K, 61, 62, 63, 78 Chen, H, 165, 184 Chen, L J, 174, 185 Choo, T K D, 62, 78 Chou, Y K, 70, 71, 78 Clark, I E, 59, 78 CMTI APT 300, 202 CMTI Handbook, 192, 193, 194, 216, 229, 230, 282 CMTI Bangalore, 401, 403 406, 407 Colibri, 307 309, 362 Cook, N H, 38, 77, 143, 182 Copley Controls Corp, 206, 208, 216 Corbett, J, 198, 201, 202, 207, 208, 210, 212, 216

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Figure 1833 depicts the torque-speed characteristic of a capacitor-start motor Because of their higher starting torque, these motors are very useful in connection with loads that present a high static torque Examples of such loads are compressors, pumps, and refrigeration and air-conditioning equipment It is also possible to use the capacitor-start motor without the centrifugal switch, leading to a simpler design Motors with this design are called permanent split-capacitor motors; they offer a compromise between running and starting characteristics A typical torque-speed curve is shown in Figure 1834

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