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Related Concept Videos

Norton's Theorem01:14

Norton's Theorem

1.4K
Norton's theorem is a fundamental principle stating that a linear two-terminal circuit can be substituted with an equivalent circuit, which comprises a current source (ⅠN) in parallel with a resistor (RN). Here, ⅠN represents the short-circuit current flowing through the terminals, and RN stands for the input or equivalent resistance at the terminals when all independent sources are deactivated. This implies that the circuit illustrated in Figure (a) can be exchanged with the one depicted...
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Norton Equivalent Circuits01:16

Norton Equivalent Circuits

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Norton's theorem is a fundamental concept in the field of electrical engineering that allows for the simplification of complex AC circuits. The theorem states that any two-terminal linear network can be replaced with an equivalent circuit that consists of an impedance, which is parallel with a constant current source. Figure 1 shows the AC circuit portioned into two parts: Circuit A and Circuit B, while Figure 2 depicts the circuit obtained by replacing Circuit A by its Norton equivalent...
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Preparation of Nitriles01:12

Preparation of Nitriles

2.6K
One of the common methods to prepare nitriles is the dehydration of amides. This method requires strong dehydrating agents like phosphorous pentoxide or boiling acetic anhydride for converting amides to nitriles. Another reagent namely, thionyl chloride also accomplishes the dehydration of amides, where amide acts as a nucleophile. The first step of the mechanism involves the nucleophilic attack by the amide on the thionyl chloride to form an intermediate. In the next step, the electron pairs...
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Electrophilic Aromatic Substitution: Nitration of Benzene01:20

Electrophilic Aromatic Substitution: Nitration of Benzene

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The nitration of benzene is an example of an electrophilic aromatic substitution reaction. It involves the formation of a very powerful electrophile, the nitronium ion, which is linear in shape. The reaction occurs through the interaction of two strong acids, sulfuric and nitric acid.
8.2K
NMR Spectrometers: Resolution and Error Correction01:14

NMR Spectrometers: Resolution and Error Correction

1.0K
When magnetic nuclei in a sample achieve resonance and undergo relaxation, the signal detected in NMR is an approximately exponential free induction decay. Fourier transform of an exponential decay yields a Lorentzian peak in the frequency domain. Lorentzian peaks in an NMR spectrum are defined by their amplitude, full width at half maximum, and position, where the peak width is governed by the spin-spin relaxation time alone. In real experiments, however, the applied magnetic field is rendered...
1.0K
2° Amines to N-Nitrosamines: Reaction with NaNO201:20

2° Amines to N-Nitrosamines: Reaction with NaNO2

5.3K
Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.
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Dissolution Dynamic Nuclear Polarization Instrumentation for Real-time Enzymatic Reaction Rate Measurements by NMR
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