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The organic layer is washed using saturated sodium chloride by shaking the separatory funnel containing the solution. It allows water molecules to move from the organic layer to the aqueous layer (refer to steps 4 and 7 from Part A of the procedure). True or False? * I'm confused about this question because by shaking and washed was bolded. But we don't shake it, we invert and vent? Or am I overthinking it?
This experiment is completed over two lab periods. In the first lab period, the initial reaction mixture (pale yellow color) is placed in an Erlenmeyer flask and allowed to stir for about 15-minutes until the yellow color subsides. Which of the following is placed in the initial reaction mixture? Select all that applies:
-12 mL of acetone
-10 mL of DI water
-3.8 mL of cyclohexene
-20 mL of diethyl ether
-20 mL of saturated sodium chloride
-a dime sized portion of anhydrous sodium sulfate
-7.4 g of N-bromosuccidimide (NBS)
Consider the reaction scheme for the two step syntesis of epoxycyclohexane from cyclohexene to match each of the following:
Starting Material (step 1)
Reagent (bromine source)
Reagent (hydroxide source)
Reaction intermediate (starting material of step 2)
Product
Reagent (deprotonates the alcohol group in 2-bromocyclohexanol)
The organic layer is washed using saturated sodium chloride by shaking the separatory funnel containing the solution. It allows water molecules to move from the organic layer to the aqueous layer : True
(you are overthinking it, it is simple statement , as during separation will shake solutions in separatory funnel for better outcomes). ( The organic layer is separated from the aqueous layer : Any water present in organic layer can be removed by usig drying agent such as NaCl, wash it with saturated NaCl solution before adding drying agent. The NaCl solution transfers the water from the organic layer to the aqueous layer. )
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This experiment is completed over two lab periods. In the first lab period, the initial reaction mixture (pale yellow color) is placed in an Erlenmeyer flask and allowed to stir for about 15-minutes until the yellow color subsides. Which of the following is placed in the initial reaction mixture? Select all that applies:
-12 mL of acetone
-10 mL of DI water
-3.8 mL of cyclohexene
-7.4 g of N-bromosuccidimide (NBS)
Consider the reaction scheme for the two step syntesis of epoxycyclohexane from cyclohexene to match each of the following:
Starting Material (step 1) : cyclohexene
Reagent (bromine source) : N-bromosuccidimide (NBS)
Reagent (hydroxide source) : water
Reaction intermediate (starting material of step 2) : 2-bromocyclohexanol
Product : epoxycyclohexane
Reagent (deprotonates the alcohol group in 2-bromocyclohexanol) : OH- (base : NaOH )
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Post Lab Questions what is the purpose of glacial acetic acid in this reaction? (5 points) 2. How does KI-starch paper work? What is the source of the dark color 3. What is the purpose of adding saturated aqueous sodium bisult What reaction is taking place? Write out the bar my saturated aqueous sodium bisulfite to the reaction mixture? is taking place? Write out the balanced equation for this reaction. Why do you e kl-starch paper test after adding the...
Thumbs up for good answer. Why does the liquid in the round bottom flask turn light pink?, please explain (This happened during/after step 2). This is the procedure and the experiment is called Synthesis of Artificial Flavorings by Fischer Esterification. Thank you! SAMPLE PROCEDURES: 1. Isoanvl acetate (banana) + H2O OH HO 1. Mix 6 mL of isoamyl alcohol (0.809 g/mL, 88.148 g/mol) and 10 ml ofglacial acetic acid (1.05 g/ml 60.05 g/mol) in a 100 mL round bottom flask....
Experiment . the reduction of bencil (March 2020) Your name Sodium borohydride is a convert recent for the reduction of dehydes and ketones to 1" and 2 alcohols, respectively. The mechanism of the reaction - (below) is straightforward and is driven by boron's affinity for oxygen. In addition, given borohydride's remarkably low reactivity with OH groups under neutral and especially basic conditions, this reaction can be done in alcohol solvents. This means that (unlike LAH or Grignard reactions) no separate...
hello, i need help with the questions in the second photo Experiment 6. the reduction of bencil (March 2020) Your name Sodium borohydride is a convert recent for the reduction of dehydes and ketones to 1" and 2 alcohols, respectively. The mechanism of the reaction (below) is straightforward and is driven by boron's affinity for oxygen. In addition, given borohydride's remarkably low reactivity with OH groups under neutral and especially basic conditions, this reaction can be done in alcohol solvents....
A Grignard reaction was performed using the following steps: Step 1: Addition of Grignard Reagent: Phenyl Magnesium Bromide a solution of phenyl magnesium bromide (2.7 mL of a 3.0 M solution in anhydrous diethyl ether) and 5 mL of anhydrous diethyl ether was dispensed into the round-bottom flask and stirred with a stir bar. Step 2: Addition Formation: Reaction with Benzophenone A solution of 0.72 g (mp = 48-49 degrees C) of benzophenone and 2.0 mL of anhydrous diethyl ether...
I was wondering if anyone could help with finding the theoretical yield? i need to get the Limiting Reagent to find the theoretical yield. it would be appreciated thanks! cyclohexanol MW: 110.16 cyclohexene MW: 82.14 Walol. 2. Cyclohexanol and especially cyclohexene are flammable liquids. Do not heating source in this experiment som stalo tento omos nopo of videos bos bosohoo Physical constants Cyclohexanol Cyclohexene bp (°C) 161 density (g/mL) 0.960 0.810 83 Experimental Procedure (macroscale) Add 20 mL of cyclohexanol...
Just Answer Question 5 Synthesis of 2-chloro-2-methylbutane (literature version) Concentrated aqueous hydrochloric acid (HCI, 3.3 equivalents) was slowly added to 2-methyl-2-butanol (1.0 equivalents) in a 100 mL round bottom flask with stirring. The reaction was stirred for 15 minutes at room temperature. Upon completion, the reaction mixture was transferred to a 60 mL separatory funnel and the aqueous layer was removed. The organic layer (i.e. the product) was successively washed with: (1) saturated aqueous NaCl (brine), (2) saturated aqueous NaHCO,...
Please help! i will give a thumbs up immediately! From any source you like, choose a natural product (an organic compound or substance produced by a living organism that is found in nature) with not more than 18 and not less than six carbon atoms. Draw the structure of your compound including stereochemical information, report a name, the molecular formula and molar mass. (5 pts.) Cite one publication that describes the synthesis of this molecule, check e. g. Google Scholar....
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(If you need any more information just let me know) Determine the limiting reagent for the preparation of 2-bromo-2-methylbutane and calculate the theoretical yield of product. 1 CHEM-2223 Organic Chemistry Laboratory I Exp. 7: Synthesis of 2-chloro-2-methylbutane In this reaction a tertiary alcohol, 2-methyl-2-butanol, is converted to a tertiary halide, 2-chloro- 2-methylbutane through a SN1 reaction. 1) Chemicals 2-Methyl-2-butanol Hydrochloric acid, HCl (12 M) Saturated sodium bicarbonate Saturated sodium chloride (380 g/L) Anhydrous sodium sulfate...