Aldehyde and Ketone 1. ALDEHYDE Definition: An aldehyde is an organic compound containing a formyl group. This functional group‚ with the structure R-CHO‚ consists of a carbonyl center (a carbon double bonded to oxygen) bonded to hydrogen and an R group‚ which is any generic alkyl or side chain. The group without R is called the aldehyde group or formyl group. Aldehydes differ from ketones in that the carbonyl is placed at the end of a carbon skeleton rather than between two carbon atoms
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ALDEHYDES AND KETONES Abstract Aldehydes and Ketones have certain characteristics in common. However‚ both couldn’t exist in the same compound. Some test for the presence of aldehyde was made for this experiment. These tests includes Tollen’s test‚ Benedict’s Test‚ 2-4-dinitrophenylhydrazine and Schiff’s test. All the tests conduted yielded same results‚ that is‚ formalin and benzaldehyde are aldehyde-containing compounds while acetone is a ketone. On the other hand‚ effect of acid concentration
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Analysis of Alcohols‚ Aldehydes and Ketones Karl Wayne Mancao‚ Raphaell Mordeno‚ Andres Pastrana III*‚ and Shannen Peñaverde Department of Biology‚ University of Santo Tomas‚ Manila‚ Philippines Abstract The proponents have done several tests for identifying alcohols‚ aldehydes and ketones. These tests are Dichromate test‚ Tollens test‚ Lucas test‚ DNPH test and Iodoform test. Three samples got positive result in dichromate test and one in Tollens test. Lucas test got one sample that has
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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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Abstract: A qualitative analysis experiment was conducted to determine the identity of an unknown aldehyde or ketone. The tests include a Tollens test‚ a Schiff test‚ an iodoform test‚ and a derivative melting point test. The data of the first three tests was inconclusive. The final derivative melting point test was utilized to successfully determine that the unknown was the ketone‚ Propiophenone. Introduction: Qualitative analysis is a method or series of methods used to determine the
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E. Reactions of Aldehydes and Ketones with Sodium Hydroxide Objectives: To know the reactions of aldehydes and ketones with sodium hydroxide a) State the function of Sodium Hydroxide in the test. Sodium hydroxide (NaOH) is the oxidizing agent. b) What are the principles involved in the test? What is its purpose? Cannizzaro reaction is a reaction that uses a strong base‚ such as sodium hydroxide‚ which results to the formation of a carboxylic acid (or its corresponding salt) and an alcohol
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Reactions of Carbonyls-Aldehyde/Ketone Analysis: Introduction: The carbonyl group is a rich source of many important reactions in organic chemistry‚ with two fundamental properties that are primarily responsible for its diverse chemistry. The first is the polarization of the. Carbon-oxygen pi bond‚ owing to the relatively high electro negativity. The second property of a carbonyl function is to increase the acidity of the alpha-hydrogen atoms‚ which are the hydrogen’s
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Laboratory #6 Qualitative Tests for Carbonyls: Aldehydes vs. Ketones Introduction Various chemical tests identifying ketones and aldehydes are used in this experiment in order to identify an unknown carbonyl compound. The tests used are: 2‚4-dinitrophenylhydrazone test‚ Tollen’s Test‚ Benedict’s Test‚ Chromic Acid Test‚ aka Bordwell-Wellman Test‚ Schiff’s Test‚ and Iodoform Test. These classification tests provide results based on color change or formation of precipitation‚ which is then used
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on the aromatic aldehyde affect the E/Z ratio of products that form. In this experiment‚ a nitro group was used as the substituent in the ortho‚ meta and para positions‚ with benzaldehyde as the control. Each of the four aldehydes reacted with (carbethoxymethylene) triphenylphosphorane to produce ethyl cinnamate‚ ethyl-3-(2-nitrophenyl)acrylate‚ ethyl-3-(3-nitrophenyl)acrylate‚ and ethyl-3-(4-nitrophenyl)acrylate. The prediction was the closer the substituent was to the aldehyde‚ the greater the
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Flavoring Agents made from Aldehydes and Ketones Peter Konn Mountain State University Chemistry 302 7/31/12 Abstract This paper looks to delve into the chemistry behind ketones and aldehydes as well as related compounds. The endeavor involved looking into the way their bonding influences how they react. It also considers the simple physical properties of these compounds including their reaction with other compounds‚ chemical structures and formulas. The paper also looked to
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