Attached below are the pages from this lab report to help give context to the questions. Please be as detailed as possible when answering the questions and include any relevant information about intermolecular forces at play. Thank you for your help!



Here are the questions which I need answered. Thank you in advance for your help! :) Please be as detailed as possible and discuss any intermolecular forces in detail if they are relevant to the question. Thanks!

Following is the Answer & Solution to Question - 1 of the given Question Set , in image format...





Attached below are the pages from this lab report to help give context to the questions....
Draw an extraction flow chart for the Extraction experiment you completed. experiment below Separation of a Benzoic Acid/Biphenyl Mixture by Acid-Base Extraction Prepare the solution to be extracted by dissolving 2.5 g of a 1:1 mixture of benzoic acid/ biphenyl in 25 mL of tert-butyl methyl ether (MTBE) . Using a 125 mL separatory funnel extract the ether solution with a mixture containing 10 mL of distilled water and 15 mL of saturated NaHCO3 . Repeat After removing the aqueous...
Would the methylene chloride layer be above or below the experiment? Justify your answer. 1. aqueous layer in today's ium carbonate used in the isolation of caffeine? Be specific as to the 2. Why is potass chemical species the carbonate may act on. Why was sodium sulfate used? 3. 4. After introducing 1.0 g of potassium carbonate into the centri hot water extract, it was capped, shaken, and then cooled to room temperature. Following this, roug minute. Why wasn't the...
The alcohol could easily be converted to a tosylate, a good
leaving group, and a conventional substitution reaction could have
been performed instead of the nucleophilic aromatic substitution
(NAS) reaction. Why was the NAS reaction the preferred method?
(Hint : Look up the nucleophiles of both reactions on chemical
manufacturing site.)
Part A: Synthesis of (t)-N,N-dimethyl-3-phenyl-3-(4- trifluoromethylphenoxy)propanamine 1. To the 250-mL round-bottom flask (RBF) containing (t)-3-(dimethylamino)-1-phenylpropanol (product from Lab 6) and a magnetic stir bar, add 4 mL of 4-...
Draw a flowchart for the flowing extraction: When the residual magnesium has all dissolved, transfer the mixture to a separatory funnel and separate the layers [Technique 10.3]. Keep both layers. Return the aqueous layer to the funnel and extract it twice with 25-mL portions of ether. Combine the two ether extracts with the ether layer from the first separation and dry the combined ether solution with anhydrous potassium carbonate. Set the aqueous layer aside for later neutralization.
Create a separation scheme flow chart/diagram to isolate methyl salicylate from a product mixture containing the following: Methyl salicylate, methanol, concentrated sulfuric acid. Lab procedure for separation: Extract with 25mL dichloromethane. Drain the bottom organic layer into a beaker. Repeat the extraction with another 25mL portion of dichloromethane, isolate the bottom layer, and then combine it with the first dichloromethane extract. Pour the combined extracts back into the funnel and wash the solution with 25mL of water. Drain the lower...
Extraction of solids: Experiment outlined below
Draw a “roadmap” of the experiment, containing chemical
structures and “layers” (organic and aqueous). This should contain
the individual reactions occurring in each step, and show which
layer the various components are present. Make sure you think about
whether the acetaminophen, caffeine and aspirin are neutral,
protonated or deprotonated.
Preliminary separation obtain a sample (1.0g) of the mixture. weigh the sample and record it. this sample should consist of a 2:1:1 mixture (by mass)...
An unknown compound followed by 4.0 mL of diethyl ether were mixed and transferred to a separatory funnel. 2.0 mL of 1.0 m NaOH were added to the funnel, the bottom aqueous layer was removed and placed into an erlenmeyer flask labled NaOH extract 1, another 2.0 mL was added to the funnel and the lower aqueous layer was put into a second flask labled NaOH extract 2. The ether layer was left in the flask. 1. What compound was...
Construct a flow chart describing the seperation of the
mixture and the isolation of each compound in this experiment. (Lab
steps/procedures includes for reference)
4. Construct a flow chart describing the separation of the mixture and the isolation of each compound in this experiment. A commonly used method of separating a mixture of organic compounds is known as liquid-liquid extraction. Most reactions of organic compounds require extraction at some stage of product purification. In this experiment you will use extraction...
The alcohol could easily be converted to a tosylate, a good
leaving group, and a conventional substitution reaction could have
been performed instead of the nucleophilic aromatic substitution
(NAS) reaction. Why was the NAS reaction the preferred method?
(Hint : Look up the nucleophiles of both reactions on chemical
manufacturing site.)
Part A: Synthesis of (t)-N,N-dimethyl-3-phenyl-3-(4- trifluoromethylphenoxy)propanamine 1. To the 250-mL round-bottom flask (RBF) containing (t)-3-(dimethylamino)-1-phenylpropanol (product from Lab 6) and a magnetic stir bar, add 4 mL of 4-...
Need help on providing reactions that describe the acid-base
extraction and neutralization processes used in this experiment.
Provide a statement of solubility of each starting material and
product.
The experiment to be performed this week involves liquid-liquid extraction using a separatory funnel. Read chapter 15 in Zubrick to familiarize yourself with the use of the glassware for extraction and washing. Acid/Base Extraction Liquid-liquid extraction is a technique that can be used to physically separate two substances that have varying solubility...