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Reaction that goes

Look again at Figure 16-1 If two NO2 molecules can form a bond when they collide, then that bond also can break apart when an N2 O4 molecule distorts. The concept of reversibility is a general principle that applies to all molecular processes. Every elementary reaction that goes in the forward direction can also go In the reverse direction. As a consequence of reversibility, we can write each step in a chemical mechanism using a double arrow to describe what happens at chemical equilibrium. [Pg.1139]

C17-0126. In each of the following situations, one reaction goes essentially to completion. In each case, identify the major species in solution under initial conditions and write a balanced net ionic equation for the reaction that goes essentially to completion, (a) Gaseous HBr is bubbled through a 0.015 M solution of Ca (0H)2. (b) 4.0 g of NaOH is added to 0.75 L of 0.055 M NaHSOq. (c) 25.0 mL of saturated NIL) I is mixed with 50.0 mL of 0.95 M Pb (N03)2. [Pg.1271]

As described in Chapter 4, acid-base reactions that go to completion can be exploited in chemical analysis using the method of titration. Titrations can be understood in greater detail from the perspective of acid-base equilibria. Protonation of a weak base by a strong acid is a reaction that goes virtually to completion because of its large... [Pg.1290]

Compare a system at equilibrium to a reaction that goes to completion. [Pg.141]

Write a generalized equation to show the relationship between reactants and products in a reaction that goes to completion because of the formation of a precipitate. [Pg.142]

In electroanalysis, the techniques are pre-eminently based on processes that take place when two separate poles, the so-called electrodes, are in contact with a liquid electrolyte, which usually is a solution of the substance to be analysed, the analyte. By means of electrometry, i.e., by measuring the electrochemical phenomena occurring or intentionally generated, one obtains signals from which chemical-analytical data can be derived through calibration. Often electrometry (e.g., potentiometry) is applied in order to follow a reaction that goes to completion (e.g., a titration), which essentially represents a stoichiometric method, so that the electrometry merely acts as an end-point indicator of the reaction (which means a potentiometric titration). The electrochemical phenomena in electroanalysis, whether they take place in the solution or at the electrodes, are often complicated and their explanation requires a systematic treatment of electroanalysis. [Pg.20]

A reagent in solution can enhance a mass transfer coefficient in comparison with that of purely physical absorption. The data of Tables 8.1 and 8.2 have been cited. One of the simpler cases that can be analyzed mathematically is that of a pseudo-first order reaction that goes to completion in a liquid film, problem P8.02.01. It appears that the enhancement depends on the specific rate of reaction, the diffusivity, the concentration of the reagent and physical mass transfer coefficient (MTC). These quantities occur in a group called the Hatta number,... [Pg.814]

The proeess produces only ethylene in a reaction that goes to completion with a feed of 5 mole % C2H6 in air in an adiabatic CSTR operated at a pressure of 2 atm with r = 10 min. We find that the reaetion rate is given approximately by the expression... [Pg.265]

Is the reaction that goes on in a hydrogen-oxygen fuel cell an example of electrolysis ... [Pg.378]

Another related reaction that goes through a ketimine is the conversion of the amino acid kynurenine to alanine and anthranilic add.225 It presumably depends upon hydration of the carbonyl group prior to P cleavage (Eq. 14-35). An analogous thiolytic cleavage utilizes CoA to convert 2-amino-4-ketopentanoate to acetyl-CoA and alanine.226... [Pg.746]

The (EiCBJjp mechanism is a close cousin of the (E1cB)b mechanism. The difference is that in the former the free anion is not formed but exists as an ion pair with the protonated base as counter-ion. An example of a reaction that goes by this mechanism is the formation of bromoacetylene from cis-l,2-dibro-moethylene and triethylamine (Equation 7.31).77 If the rate of elimination from deuterated 1,2-dibromoethylene is compared to the rate from nondeuterated material, kHlkD x 1. Therefore proton abstraction is not involved in the ratedetermining step. Because added Et3 D X- does not affect the rate and be-... [Pg.360]

The equation AG° = —RT In K is one of the most important relationships in chemical thermodynamics because it allows us to calculate the equilibrium constant for a reaction from the standard free-energy change, or vice versa. This relationship is especially useful when K is difficult to measure. Consider a reaction so slow that it takes more than an experimenter s lifetime to reach equilibrium or a reaction that goes essentially to completion, so that the equilibrium concentrations of the reactants are extremely small and hard to measure. We can t measure K directly in such cases, but we can calculate its value from AG°. [Pg.747]

Stars are made up of mostly hydrogen and helium. They also contain some other elements in small quantities. The brightness of a star is due to the continuous nuclear reaction that goes on in its core. During this reaction, hydrogen is converted to helium and tremendous energy is released. Stars shine due to this heat. Our sun is only an average star. Yet, the temperature at its core is 15,000,000°C. [Pg.170]

Decomposition reactions are often involved in thermal explosions or runaway reactions, in certain cases as a direct cause, in others indirectly as they are triggered by a desired synthesis reaction that goes out of control. A statistical survey from Great Britain [1, 2] revealed that out of 48 runaway reactions, 32 were directly caused by secondary reactions, whereas in the other cases, secondary reactions were probably involved too, but are not explicitly mentioned (Figure 11.1). Therefore, characterizing secondary decomposition reactions is of primary importance when assessing the thermal hazards of a process. [Pg.283]

A normal kinetic isotope effect has k /ko > 1. Deuterium Is often put into compounds by exchange with the cheapest source. D20, so reactions in D20 often go slower than reactions in H20. Reactions with k /ko < 1 have inverse deuterium isotope effects so a reaction that goes faster in D2Othan in H20 (even when that is the expected pattern) has an inverse solvent deuterium isotope effect. [Pg.1103]

Why is this important Well, if you cast your mind back to Chapter 38, you will remember that tlie overlap of parallel orbitals was very important in fragmentation reactions. Here, for example, is a fragmentation reaction that goes very well, but that can take place only if the nitrogen s lone pair is equatorial, because only an equatorial (black) lone pair can overlap with the antibonding orbital of the C-C bond that breaks. The chloride leaving group must be equatorial as well. [Pg.1128]

The idea of coupling two keto-esters together with a nitrogen atom also works for pyridines except that an extra carbon atom is needed. This is provided as an aldehyde and another important difference is that the nitrogen atom is added as a nucleophile rather than an electrophile. These are features of the Hantzsch pyridine synthesis. This is a four-component reaction that goes like this. [Pg.1191]

Another reaction that goes better with thiol esters than with ordinary esters is enolization. This is an equilibrium reaction and the enol has lost the conjugation present in the ester. The thiol ester has less to lose so is more enolized. This is the reaction of acetyl CoA that we are now going to discuss. We have mentioned the citric acid cycle several times and it has appeared in two... [Pg.1389]

If, when two solutions are mixed, a reaction that goes virtually to completion occurs, it is essential to do the stoichiometric calculations before considering the equilibrium calculations. In this case we let the system go completely in the direction toward which it tends. Then we let it adjust back to equilibrium. If we let Pb2+ and I- react to completion, we have the following calculations ... [Pg.326]

Psoralens (obtained from citrus fruits and other plants), e.g. methoxsalen, are used to induce photochemical reactions in the skin. After topical or systemic administration of the psoralen and subsequent exposure to UVA there is an erythematous reaction that goes deeper than ordinary sunburn and that may reach its maximum only after 48 h (sunburn maximum is 12-24 h). Melanocytes are... [Pg.306]


See other pages where Reaction that goes is mentioned: [Pg.124]    [Pg.347]    [Pg.598]    [Pg.437]    [Pg.110]    [Pg.34]    [Pg.1740]    [Pg.359]    [Pg.129]    [Pg.978]    [Pg.21]    [Pg.337]    [Pg.683]    [Pg.429]    [Pg.264]    [Pg.8]    [Pg.230]    [Pg.89]    [Pg.978]    [Pg.978]   
See also in sourсe #XX -- [ Pg.418 ]




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