
Oeganic chemistry questions ORGO HOMEWORK #2: A SEPARATION As this nightmare develops, the only way I...
Steps for the separation by extraction of benzil? What order of steps do I need to place it in? Describe the procedure for the separation by extraction of the neutral compound, benzil, from the basic compound, p-chloroaniline. Both compounds are soluble in dichloromethane and insoluble in water. At the end of the prodecure, you must have solid benzil and solid p-chloroaniline separated Note: dichloromethane is a highly volatile solvent, thus if you boil a solution of a compound in dichloromethane...
Hello, I need help understanding a lab we are doing in class tomorrow. I need to know which is the "ORGANIC LAYER" ... we are using a separatory funnel, and I would like to know whether the organic layer will be on top or on the bottom. This is in order for me to correctly carry out the experiment. The lab is similar to this one I found online, and its very vague for me as to what is the...
Name: Date: Separation of Acid/Base/Neutral compounds using liquid-liquid extraction OCH CHO HN Benzocaine Molecular Weight: 165.19 Melting Point: 88-90 °C 1,1-biphenyl Molecular Weight: 154.21 Melting Point: 68-70 °C trans-cinnamic acid Molecular Weight: 148.16 Melting Point: 132-135 °C Question 1: Identify the following compounds as Acid, Base or Neutral. (2 points) a. Benzocaine: b. Biphenyl: c. Trans-cinnamic acid: (2 points) _ (2 points) Question 2: Draw the structure in the box (5 points each): NaOH OCH,CH, HCM NaOHA HC form. Ples...
can someone help with orgo homework 2 and 3 please. currently I
think 2 is A.
for three I have
A D
B C
thanks!!!!
2. Which of the choices below correctly ranks the groups in terms of priority in the RS system? -CH2CH=CH2 -CH=CH2 -CH2C-OH -CH2OH Ans. - @@@@@@@ NWAW MNNNM APAwwNN NW 3. (20 pts.) Identify the relationship between the molecules in each of the following pairs by writing the CAPITAL LETTER of the best answer. You may...
2) You are presented with an unknown that possibly has Ag-, Bi-, Sn+, Zn2+, Co2+ and Na'. You divide the solution into three equal volumes, labeling one "A," one "B," and one "C." To "A" you add 6 M HCl and do not observe any precipitate forming. In tube B, you add 6 M HCl until the pH is 0.5 then add thioacetamide and heat the solution in a hot water bath for seven minutes, eventually observing a black precipitate....
ORGANIC LAB: Separating a Mixture of two Unknowns, different acidity I have a mixture of two unknowns, both solids, in my Organic Chemistry lab. I have to separate them, then find out what each compound is. The only thing I really have that I can go by is that they have different acidities, each is either an acid (weak or strong), a base, or a neutral, and one can't be what the other is. I found a separation technique that...
ORGANIC LAB: Separating a Mixture of two Unknowns, different acidity I have a mixture of two unknowns, both solids, in my Organic Chemistry lab. I have to separate them, then find out what each compound is. The only thing I really have that I can go by is that they have different acidities, each is either an acid (weak or strong), a base, or a neutral, and one can't be what the other is. I found a separation technique that...
can you pleas help me making a Flow chart for separation a
mixture of trans-cinnamic acid,
4-phenylphenol, and nicotinamide by extraction?
thank you
Procedure Your mission is to separate a mixture of trans-cinnamic acid, 4-phenylphenol, and nicotinamide by extraction. Start by dissolving/suspending two grams of the mixture in approximately 50 mL of diethyl ether. (Caution: Diethyl ether is extremely flammable! Extract the ether twice with -25 mL of 5% HCl and then twice with -25 mL 5% sodium bicarbonate. It...
Acid/Base Extraction
ACID/BASE EXTRACTION Provide a flow chart detailing the acid/base extraction/separation of the compounds shown below. Your answer must employ the following reagents: methylene chloride, hydrochloric acid (1M & 6M), sodium hydroxide (1M & 6M), 10% sodium bicarbonate (aq). Clearly indicate the product(s) and layers formed following each step of your separation scheme. HINT: phenol is soluble in sodium hydroxide solution but insoluble in neutral water or sodium bicarbonate solution. Benzoic acid is soluble in both sodium hydroxide and...
please help with these chemistry problems
2. (5 points) Why does this reaction occur via a Si1 pathway and not via a Si2 pathway? 3. (5 points) In general are SN1 reactions stereospecific? Why or why not? 2 5.(5 points) Why do carbon substituents stabilize a carbocation and destabilize a carbanion? 6. (5 points) The mass spec of your product has a base peak at 77 draw what this fragment looks like. What would explain the peak at 79. (you...