D. REACTIONS OF ALDEHYDES AND KETONES WITH SODIUM HYDROXIDE (By: Mary Deo Luigi J. Mabunay 1N-3) Objective: To determine the reactions of Aldehydes and Ketones when combined with Sodium Hydroxide. Process: * Obtain 5 clean and dry test tubes * Put 2mL of 40% NaOH solution to test tubes 1‚ 2 and 3 and on test tubes 4 and 5‚ put 10% NaOH solution * Add 10 drops of the following solution: * Tube 1: formaldehyde * Tube 2: benzaldehyde * Tube 3: acetaldehyde
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experiment teaches the students how to determine density‚ volume‚ and percentage errors. OBJECTIVE The objective of this experiment is to determine the order with respect to permanganate ion and to oxalic acid concentration for the reaction of potassium permanganate and oxalic acid solutions. Other goals include‚ writing a rate equation and determining the effect of increased temperature on the rate of this reaction. MATERIALS AND EQUIPMENT The materials required for this experiment include
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boiling point. Through the Thomas Hoover apparatus‚ the melting point of 8 test compounds was determined. Salicylic acid exhibited the highest melting point while naphthalene‚ the lowest. The stronger the intermolecular forces of attraction‚ the higher the melting point. Boiling point determination was done on 7 different test compounds using micro method. Results show that propanoic acid and n-hexane had the highest and lowest boiling point respectively. The former had the strongest intermolecular force
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Cause and Effect on Acid Rain Introduction Beautifully crafted statues are now worn out or severely damaged‚ aquatic wildlife population are dying off‚ forests have lost the leaves that protect their trees and produce food‚ and the rates of lung diseases in humans are rising around the world. The cause of all of these problems can be linked back to acid rain. Most people don’t understand the concept or science behind acid rain. The common belief is that it’s a natural process‚ but it’s actually
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RESULTS AND CALCULATIONS Ligroin Toluene Ethanol H2O Anthracene Did not dissolve Slightly dissolved Did not dissolve Did not dissolve Benzoic acid Did not dissolve Dissolved Slightly dissolved Did not dissolve Phthalic acid Almost dissolved Almost dissolved Did not dissolve Dissolved Resorcinol Dissolved Dissolved Dissolved Dissolved Sodium naphthionate Did not dissolve Did not dissolve dissolved Dissolved Table 1. Results for the five compounds tested in four different solvents. Functional Group
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Notes Aldehydes and Ketones The major similarity between an aldehyde and a ketone is the carbonyl group. A carbonyl group is a carbon atom doubly bonded to an oxygen atom. [pic] Both molecules have a carbonyl group‚ the difference the number of carbons bonded to the carbonyl carbon. An aldehyde will have none or one and a ketone will have two carbons. All aldehydes‚ except formaldehyde‚ will have a hydrogen atom on one side of the carbonyl carbon and at least on carbon on the other side
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Acid in the human stomach When people refer to acid they usually see it as a corrosive liquid that can dissolve metals or change the color of a substance. So they think of acid as a dangerous matter for the body and believe it can easily dissolve your skin. What I have previously listed are indeed properties of certain acids‚ such as Hydrofluoric Acid which can cause irreversible tissue damage if it comes in contact with skin‚ but not all acids are this strong. As a matter of fact what a lot of
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Acids and Bases Shane Purpose- To study the relationship between pH and metabolism. 10/21/13 Materials- see attached Per. D Biology Procedure- see attached Data and Results- see attached Theory- PH stands for the power of hydrogen. People refer to the pH scale as a tool for finding out if a substance is acidic‚ basic‚ or neutral. This scale goes from zero to fourteen. The number seven is neutral. Any number higher than seven on this scale is basic. Any number lower is acidic
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FREQUENCIES (bend) Aromatic (stretch) (out-of-plane bend) Alkyne Aldehyde C=C C C C=O (stretch) Alkene (stretch) Aromatic (stretch) Alkyne (stretch) Aldehyde (stretch) Ketone (acyclic) Carboxylic Acid Ester Amide Anhydride Alcohols‚ ethers‚ esters carboxylic acids Alcohols‚ phenols Free H-bonded Carboxylic acids Primary and secondary amines Nitriles Nitro C-O O-H NH C N N=O 3650-3600 3400-3200 3300-2500 ca. 3500 2260-2240 1600-1500 and 1400-1300 m m m m m s -OH‚ -NH CHEMICAL SHIFTS
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Reducing Sugars : Sugars that contain aldehyde groups that are oxidised to carboxylic acids are classified as reducing sugars. Common test reagents are : Benedicts reagent (CuSO4 / citrate) Fehlings reagent (CuSO4 / tartrate) They are classified as reducing sugars since they reduce the Cu2+ to Cu+ which forms as a red precipitate‚ copper (I) oxide. Remember that aldehydes (and hence aldoses) are readily oxidised (review ?) In order for oxidation to occur‚ the cyclic form must first ring-open
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