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: Synthesis of Nylon (Polyamide) ~ Pre-Lab Assignment Section #- Score - Nylon 6-6 is a...
I. Nylon 6-6 is a condensation polymer. The last two lab handouts pointed out that "condensation reactions are extremely common among a variety of organic functional groups." Pick two appropriate functional groups (your choice) and draw structures to show the condensation reaction between them. Identify the functional groups that are reacting, as well as the linkage formed by the condensation. 2. Rather than use a carboxylic acid for the nylon condensation, you'll use the more reactive acid chloride. This must...
Discussion Questions The structures of acetanilide and malonic acid are provided below 1. For each structure, draw circles around the polar and nonpolar regions of the molecule, and label each circled regiorn with the type of intermolecular attractive force it can use to interact with other molecules. Acetanilide Malonic Acid но CH2 OH 2. Now-thoroughly explain (on the basis of polarity/nonpolarity and intermolecular attractive forces) how the acetanilide was separated from the malonic acid by recrystallization from water. And explain...
Hello I need some help with these organic chem pre lab questions for the extraction of trimyristin from nutmeg 4.(1) What technique is used to ensure as much as possible trimyristin is extracted from the nutmeg? 5. (6 pts.) Indicate whether the following statements are true (T) or false (F) AND correct any of the false statements. a. The functional group present in trimyristin is a carboxylic acid group b. Pure trimyristin is a liquid at room temperature. c. The...
4 Synthesis of lohexene by Dehydration - Pre-Lab Assignment de drated with a strong and high A w a y 's G UPAC 3) Explain why two products are formed from the dehydration of 3-hexanol, but only ONE product is formed from the dehydration of 3-pentanol. (Consider tr a d isomers only, not cis/trans stereoisomers.) 2. In an organic synthesis, reactions are sometimes performed in sequence to convert one functional group into another Complete this multi-step reaction sequence on paper:...
what is the theoretical yield for this experiment? ORGANIC POLYMERS: THE SYNTHESIS OF NYLON Nylon's outstanding characteristic in the textile industry is its versatility. It can be made strong enough to stand up under the punishment tire cords must endure, fine enough for sheer, high fashion hosiery, and light enough for parachute cloth and backpacker's tents. Nylon is used both alone and in blends with other fibers, where its chief contributions are strength and abrasion resistance. Nylon washes easily, dries...
Experiment #6 Ester Synthesis PRE-LAB ASSIGNMENT This pre-lab assignment is worth 5 points for this Experiment and should be completed on a separate page and turned in at the beginning of lab. 1. Read the experiment carefully 2. Safety Considerations: Summarize O safety and health hazards for working with glacial acetic acid, butanoic acid and petroleum ether. 3. Procedure: Summarize the procedure using a bullet list. Assume you are summarizing the procedure to a fully qualified chemist, i.e. don't include...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
**(left structure)****(right structure)** The two structures for the assignment are above and the task is: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends upon the target. For the structure given above (structure on left), the starting material is either malonic ester or acetoacetic ester and any halide. For the structure given above (structure on right), the starting material is any...
Questions and Problems 553 ation for the reaction that would produse cach of the following amines b. N.Methylpropanamine c. N.N-Diethylpentanamine 15.37 Briefly explain why the lower molar massamines (lewer than five carbons) exhibit appreciable solubility in water 15.38 Why is the salt of an amine appreciably more soluble in water than the mine from which it was formed 15.39 Most drugs containing amine groups are not administered as the mine but rather the amount you suggeste son why? 15.40 Why...
Synthesis using Carbonyla-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. My two target molecules are number 2 and number 12 in the last page. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the...