One of the reactions you observed resulted in this product: NaCl + H2O + CO2 (g)? What well did this reaction occur in? Describe how the observations for this reaction support your answer. B BoldI ItalicsU Underline Bulleted list Numbered list Superscript Subscript70 Words A reaction I observed in number 1.) Sodium Bicarbonate mixed with Hydrochloric acid.
Danielle Pitter CHEM 137 Professor D’Amelia 3/1/17 Extraction of a Neutral Compound from Acid and Base Impurities Discussion: The diethyl ether solvent is nonpolar; therefore, based on the expression like dissolves like, other nonpolar molecules will dissolve in it. The 9-fluorenone is a nonpolar molecule; therefore, it will dissolve in the nonpolar diethyl ether. The benzoic acid has a polar carboxyl group; however, the ring is nonpolar. The nonpolar ring in the benzoic acid is what makes it soluble in the diethyl ether. The ethyl-4-aminobenzoate is similar to benzoic acid, in that it has a nonpolar ring and has polar attachments.
We concluded that the rate of hydrolysis of (CH3)3CCl is directly proportional to water content in the solvent mixture. Aims of experiment • Determine the rate constants for hydrolysis of (CH3)3CCl in solvent mixtures of different composition (50/50 V/V isopropanol/water and 40/60 V/V isopropanol/water) • Examine the effect of solvent mixture composition on the rate of hydrolysis of (CH3)3CCl Introduction With t-butyl chloride, (CH3)3CCl, being a tertiary halogenoalkane, it is predicted that (CH3)3CCl reacts with water in a nucleophilic substitution reaction (SN1 mechanism), where Step 1 is the rate-determining step. The reaction proceeds in a manner as shown
In this experiment, method 1 generate a mixture of yellowish crystals and a yellowish gluey product. Using method 2, the product appear as white crystals. Given that the yellow color remain throughout the product in method 2, too much aldehyde was added. It was predicted that this was the source of error because aldehyde was a yellow liquid. In this experiment, 293 mg of aldehyde was weighted for method 1 instead of 250 mg and.
This could have been because it was more sterically hinder since the carbonyl group was connected to a primary carbon. The third ester which reacted was ethyl butanoate since it was a bit more sterically hinder than the ethyl acetate because the carbonyl group was connected to a secondary carbon. Both ethyl acetate and ethyl butanoate had electronic factors of being electron donating making the carbonyls less reactive so the order depended more on the steric factor. The slowest ester to react was the ethyl benzoate because of the greater steric hindrance since the carbonyl was connected to a benzene ring which making it hard for the nucleophile to attack. The carbonyl was directly connected to a tertiary carbon, but that was also in a ring.
Dissolution is the process that makes solutions. A solution is a homogenous mixture of two or more substances. The solute in the solution is the substance that is dissolved, while the solvent in the solution is the substance that dissolves the solute during dissolution. The question introduced in this lab is “What factors influence the rate at which one substances dissolves in another?” The three factors that affect the rate of dissolution are temperature, how much you stir the mixture, and the particle size of the substances. Temperature increases the chance of solute and solvent particles colliding with one another.
For example, dopamine has a Km of 95 and a Vmax of 11 x 105. Both of these values are fairly high and would not make an effective substrate for catechol oxidase since the enzyme has a low affinity for the substrate. An example of a good alternative substrate would be 4-methylcatechol that has a low Km of 1.1 and a Vmax of 3.4 x 105. The enzyme now has a high affinity for the substrate and therefore requires less substrate to meet its Vmax. The substrate for the sweet potato catechol oxidase is N-phenylthiourea.
and esters. In the case of hydrolytic reaction, the steam produced during the processing of food containing water causes the hydrolysis of triglycerides, resulting in the formation of free fatty acid, glycerol, monoglycerides, and diglycerides. High free fatty acid level, i.e. quantum of free fatty acids greater than 1 mg/g KOH, results in generation of high amounts of undesirable soap simultaneously with transestriﬁcation reaction. In the alkali-catalyzed process, the presence of free fatty acid (greater than 1 mg/g KOH) and water in the oil can cause high amounts of undesirable soap formation, also consuming some quantity of alkaline catalyst and reduces the eﬀectiveness, all of which result in a lower conversion.
The original reaction done by Kolbe involved the formation of sodium phenoxide through the evaporation of a molar equivalent mixture of phenol and aqueous sodium hydroxide. The hygroscopic sodium phenoxide is then heated while carbon dioxide gas is passed over the molten salt. The mixture is then further heated to give the dianion of salicylic acid along with carbon dioxide and phenol both of which distill away from the mixture. Under these
Record results to determine if HCl increases or decreases the pH of the water. 14. If the HCl in the solution increases the pH of the water, it shows that HCl will increase the pH of the blood and if the HCl in the solution decreases the pH of the water, it shows that HCl will decrease the pH of the blood. 15. Add 10ml of 0.85% lactic acid into a beaker containing distilled water.
It is very soluble because the smaller the chain of the molecules are then the energy will be required in small quantities however if the chain is long then it will need more energy so that means that the longer chain will have a slow reaction. It does not have a color and it does not cause fires to happen. It may burn the skin because it is a corrosive substance which is why you should wear gloves when you are handling it. If you swallow the hydrogen chloride then it can be dangerous because it is a toxic substance The bonding in hydrogen chloride is called covalent bonding because nonmetals and metals have the capability to react