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Bases. reacting with

Wnte an equation for the Brpnsted acid-base reaction that occurs when each of the fol lowing bases reacts with water Show all unshared electron pairs and formal charges and use curved arrows to track electron movement... [Pg.55]

As we have seen the nucleophile attacks the substrate m the rate determining step of the Sn2 mechanism it therefore follows that the rate of substitution may vary from nucleophile to nucleophile Just as some alkyl halides are more reactive than others some nucleophiles are more reactive than others Nucleophilic strength or nucleophilicity, is a measure of how fast a Lewis base displaces a leaving group from a suitable substrate By measuring the rate at which various Lewis bases react with methyl iodide m methanol a list of then nucleophihcities relative to methanol as the standard nucleophile has been compiled It is presented m Table 8 4... [Pg.337]

FIGURE 8 11 When a Lewis base reacts with an alkyl halide either substitution or elimination can occur Sub stitution (Sn2) occurs when the Lewis base acts as a nu cleophile and attacks carbon to displace bromide Elimi nation (E2) occurs when the Lewis base abstracts a pro ton from the p carbon The alkyl halide shown is iso propyl bromide and elimi nation (E2) predominates over substitution with alkox ide bases... [Pg.349]

We said at the beginning of this chapter that two kinds of reactions can happen when a nucleophile/Lewis base reacts with an alkyl halide. The nucleophile can either substitute for the halide by reaction at carbon or cause elimination of HX by reaction at a neighboring hydrogen ... [Pg.383]

There is considerable evidence to indicate that the neutralization reaction occurs when any strong base reacts with any strong acid in water solution. It follows that the neutralization equation written above applies to any strong acid-strong base reaction. [Pg.82]

Further, sulphoxides are weak bases reacting with protons, for example ... [Pg.113]

Additional base reacts with HP042 to produce phosphate ion, P04 ... [Pg.585]

For instance, suppose we titrated H3P04(aq) with NaOH(aq). We assume that, up to the first stoichiometric point, each OH- ion from the base reacts with one molecule of H3P04 until all the latter has been consumed (Eq. B). In this part of the tit ration, the solution consists of H,P04(aq) and H2P04 , with the latter increasing as more NaOH(aq) is added and with the volume increasing, too. At the first stoichiometric point, the solution contains a salt of H2P04 with its characteristic pH. [Pg.585]

Anionic metal bases react with group-IIIB halides by eliminating halide anions, forming neutral, c-bonded IIIB-metal compounds ( 6.5.2.2) ... [Pg.54]

Mole ratios can be used to determine the amount of one substance needed to react with a given amount of another substance. In this experiment, you will react a substance called an acid with another substance called a base. Acids can be defined as substances that dissociate and produce hydrogen (H+) ions when dissolved in water. Bases are substances that ionize to produce hydroxide (OH ) ions when they dissolve in water. When acids and bases react with each other, the H+ ions and OH ions join to form water (H20). The resulting solution no longer has an excess of either H+ ions or OH- ions. The solution has become neutral. This process is called neutralization. By using the mole ratio of hydrogen ions and hydroxide ions in the balanced chemical equation, you can predict the point at which a solution becomes neutral. [Pg.93]

Naming bases is a little more straightforward. For a base name, chemists just use the name of the chemical compound. They do the same thing for the salts that are produced when acids and bases react with one another. The salt sodium chloride (NaCl), for example, is named for the two elements that are present in the salt—sodium and chlorine. The only rule is to change the ending for the name of the nonmetal (in this case, chlorine) to -ide, giving us the name sodium chloride. [Pg.28]

Ans. 2.40equivalents of base reacts with 2.40equivalents of acid, no matter what the base. [Pg.242]

Thus far, we have used the Arrhenius theory of acids and bases (Secs. 6.4 and 7,3) in which acids are defined as hydrogen-containing compounds that react with bases. Bases are compounds containing OH" ions or that form OH- ions when they react with water. Bases react with acids to form salts and water. Metallic hydroxides and ammonia are the most familiar bases to us. [Pg.302]

When the log rate constants were subjected to an excess acidity analysis, log k - log Ch+ - log h2o was found to be linear in X in both cases, whereas log k - log Ch+ was not. This again suggests the involvement of a water molecule in the rate-determining step, probably acting as a base, reacting with protonated [7] as shown in Scheme 9.248... [Pg.45]

Salts produced by a strong base reacting with a strong acid are... [Pg.307]

Bases react with an acid to form a salt and water ( neutralization )... [Pg.245]

Bases react with esters to form an alcohol and carboxylic acid ( saponification ) Bases can be corrosive... [Pg.245]

Yadav and Kapoor <2003TL8951> reported on a microwave-assisted ring closure leading to novel thiazolo[l,3,5]-triazines, as shown in Scheme 36. This three-component one-pot procedure started from the thiazolyl Schiff base 230, to which ammonium acetate and an aldehyde was added. In the first step, the azomethine moiety of the Schiff base reacted with ammonia to give the zwitterionic first intermediate 231, which underwent deprotonation to the amine 232, and, finally, reaction of this second intermediate with the aldehyde involving the ring-closure step afforded the product 233. It is important to emphasize that the MW-assisted technique ensured high yields (76-88%)... [Pg.989]

These bases react with acid as shown below ... [Pg.138]

H (aq) Cl (aq) hJa (aq) + OH (aq) Fla (aq) "t" Cl (aq) "t" H20(r) AH = —56 kJ Subtracting spectator ions from both sides, the net ionic equation is H+(aq) -I- OH (aq) H20(f) AH = -56 kJ Different combinations of strong Arrhenius acids and bases react with the same exothermic result. Measurements always show the release of 56 kJ of energy per mole of water formed. This makes sense, because the net ionic equation is the same regardless of the specific neutralization reaction that occurs. [Pg.379]

You know that 20 mL of 0.20 mol/L NH3(aq) base reacts with 0.20 mol/L HCl(aq). Tables of and values are in Appendix E. Figure 9.3 shows the pH ranges and colour changes for various indicators. [Pg.426]

We believe that the intermediate generated by anodic oxidation of 3 is the cation 3a and not nitrilimine 3b. The generation of the cation intermediate was postulated in several papers on the anodic oxidation of hydrazone derivatives [38-41], W also believe that both heteroaromatic and Schiff bases react with the cation 3a as nucleophiles rather than dipolarophiles. The most likely mechanism of the oxidation of the hydrazone 3 in the presence of heteroaromatic and Schiff bases, which would best fit the observed electrochemical and preparative results, can be described in the form of Scheme 8. [Pg.97]

In the absence of O2, the remineralization of nitrogen and sulfur generates NH3 and S. These weak bases react with the acid generated by the hydrolysis of CO2 (H2O + CO2 —> H2CO3 —> + HCOp. This titration transforms the remineralized nitrogen and sulfur... [Pg.218]

If this precaution is not followed, partial or complete equilibration of the enolates will occur because of proton transfers between the enolates and the excess un-ionized ketone. In an experiment where a slight excess of ketone was added, the distilled, monoalkylated product (40% yield) contained 77% of the undesired 2,2-isomer and only 23% of the desired 2,6-isomer. However, it is also important in this preparation not to allow a large excess of lithium diisopropylamide to remain in the reaction mixture this base reacts with benzyl bromide to form iraws-stilbene which is difficult to separate from the reaction product. [Pg.25]

Other bases found to react with 1,1,1-trinitroethane via formation of 1,1-dinitroethene include trimethylamine, guanidine and diethylmalonate anion (152), the latter forming (153) in 36 % yield. Shechter and Zeldin found no correlation as to why some bases react with 1,1,1-trinitroethane so differently to others but noted that simple alkoxides, aliphatic amines, guanidine, cyanide and malonate anions reacted via the 1,1-dinitroethene pathway. [Pg.41]

In the late 1800s, Svante Arrhenius defined an acid as a substance that increases the hydrogen ion (H ) concentration in water, and a base as any substance that increases the hydroxide ion (OH ) concentration in water. Acids and bases react with one another in a process called neutralization to form a salt and water. Hydrochloric acid neutralizes potassium hydroxide forming potassium chloride (a salt) and water ... [Pg.100]

Before the half-neutralization point, A-, formed by the addition of titrant (strong base) reacts with the excess HA to form HA2, thus the value of the [A-]/ [HA] ratio is kept lower than in the absence of homoconjugation. On the other... [Pg.73]


See other pages where Bases. reacting with is mentioned: [Pg.248]    [Pg.394]    [Pg.1182]    [Pg.1122]    [Pg.347]    [Pg.110]    [Pg.792]    [Pg.58]    [Pg.469]    [Pg.298]    [Pg.377]    [Pg.129]    [Pg.126]    [Pg.131]    [Pg.108]    [Pg.13]    [Pg.237]    [Pg.852]    [Pg.41]   


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Hydroxide ions from base reacting with

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