In this experiment the initial mass of the sodium carbonate used was 2.69g. In each titration‚ 3 drops of methyl orange was added to the sodium carbonate solution. With this information the titration can begin‚ and the results obtained are shown below: Titration readings Titration Rough 1 2 3 4 5 Initial 0.00 4.30 22.00 21.00 15.00 25.90 Final 4.30 22.00 38.60 37.60 32.60 42.20 Titre (cm3) 4.30 17.70 16.60 16.60 17.60 16.30 Therefore‚ the average titre would be calculated as follows;
Premium Titration Chemistry Mole
Objective To synthesis methyl orange by coupling diazotised sulphanilic acid with N‚N-dimethylaniline. Materials (Chemicals) Sulfanilic acid‚ 2.5% aqueous sodium carbonate solution‚ sodium nitrite‚ concentrated hydrochloric acid‚ N‚N-dimethylaniline‚ glacial acetic acid‚ 10% aqueous sodium hydroxide‚ saturated sodium chloride solution Apparatus 50 mL Erlemeyer flask‚ 250 mL beaker‚ test tube‚ hot plate‚ Buchner funnels Procedure In a 50 mL Elermenyer flask 1.2 g of sulfanilic acid and
Premium Sodium chloride Chlorine Hydrochloric acid
Forming Methyl Orange an Azo Die Abstract: An synthetic azo dye was created by reaction of diazonium salt with N‚N-Dimethylanaline. The final product created was 4-dimethylaminoazobenzene-4-sulfonic acid‚ an orange clay-like substance. Sulfanilic acid was chemically manipulated by using sodium carbonate followed by cooled sodium nitrate and hydrochloric acid to form the diazonium salt used in the reaction. The products were washed in ethanol. The product was obtained at an 84% yield and was
Premium Chemistry Hydrogen Chemical reaction
in a sample. Primarily‚ the aim of Experiment 1 was to measure the absorption spectrum of a particular coloured substance (in this case Bromophenol Blue and Methyl Orange) at varying wavelengths of light. The goal of this experiment was to measure the given amounts of a given chemical substance that was present in a given sample of Methyl Orange and in blood. We measured the optical density at wavelengths 400 to 700 in intervals of 20 mu. For Experiment 2‚ the process of the experiment focuses on
Premium Blood sugar Blood glucose monitoring Electromagnetic radiation
Tie-dye is a modern term coined in the mid-1960s in the United States for a set of ancient resist-dyeing techniques‚ and for the products of these processes. The process of tie-dye typically consists of folding‚ twisting‚ pleating‚ or crumpling fabric or a garment and binding with string or rubber bands‚ followed by application of dye. The manipulations of the fabric prior to application of dye are called resists‚ as they partially or completely prevent the applied dye from colouring the fabric.
Premium Color Color wheel Clothing
the world and sometimes different bodies have different views on food color safety. In the United States‚ FD&C numbers (which indicate that the FDA has approved the colorant for use in foods‚ drugs and cosmetics) are given to approved synthetic food dyes that do not exist in nature‚ while in the European Union‚ E numbers are used for all additives‚ both synthetic and natural‚ that are approved in food applications. The food colors are known by E numbers that begin with a 1‚ such as E100 (turmeric)
Premium Food coloring E number
spp and its application in dye decolorization Project supervisor: Dr. R. Masalu Lab scientist: Mr. Chuwa INTRODUCTION: Due to rapid industrialization and urbanization‚ a lot of chemicals including dyes are manufactured and used in day-to-day life. Dyes are synthetic and aromatic molecular structural compounds. According to their dissociation in an aqueous solution‚ dyes can be classified as acid‚ direct reactive dyes (anionic)‚ basic dyes (cationic) and disperse dyes (nonionic). They are used
Premium Dye Enzyme
In this experiment‚ we used methyl benzoate from the last experiment with HNO3 and H2SO4 to synthesize methyl 3-nitrobenzoate. First we added methyl benzoate to 12 mL cooled conc. Sulfuric acid in a flask. In a separate flask‚ we made a solution of 4 mL conc. Sulfuric acid and 4 mL nitric acid and then added dropwise to the solution of methyl benzoate in an ice bath on a stir plate while maintaining the temperature of reaction between 5-15 °C. After the addition was complete we took the flask out
Premium Water Chemistry Acetic acid
para-hydroxybenzoic acid‚ which is why they are collectively called parabens. However‚ in contrast to its cousins‚ ethylparaben‚ butylparaben‚ and propylparaben‚ methylparaben receives its specific name owing to the fact that its chemical structure contains the methyl alkyl group. Methylparaben is found in several fruits‚ in particular blueberries‚ where it acts as an antimicrobial agent. Methylparaben is an anti-fungal agent often used in a variety of cosmetics and personal-care products. Methylparaben is commonly
Premium
CARLOS DEPARTMENT OF CHEMISTRY NAME: Maniwang‚ Ma. Aiza C. DATE: March 21‚ 2011 COURSE: BS Chemistry II APPROVED: ___________ PREPARATION OF AZO DYES ABSTRACT In this experiment‚ the azo dyes p-nitrobenzene azoresorcinol and methyl orange were prepared by the azo coupling reaction. The p-nitrobenzene azoresorcinol dye was prepared from p-nitroaniline and resorcinol. The diazonium salt formed was from the reaction of the cold solution of dissolved p-nitroaniline in hydrochloric
Premium Azo compound Functional group Dye