1) C2H5Br + NaCN ----> C2H5CN + LiAlH4 ------> C2H5CH2NH2
2)(a) C6H5CONH2 is an acid derivative while C6H5CH2NH2 is an amine
Thus, cold dilute NaOH will react with the acid derivative but not with the amine
(b) Hinsbergs reagent i.e C6H5SO2Cl,OH-, then HCl will be able to distingiush between the primary and seconday amine
c) benzamine (or aniline) will form diazonium salt while cyclohexanamine will not on reaction with NaNO2,HCl
Which would yield propylamine? Two of the above All of the above Select the reagent from...
___ 13. Which reagent would best serve as the basis for a simple chemical test to distinguish between CH3CHO and CH3COCH3? A) NaOI (I2 in NaOH) B) Br2/CCl4 C) C6H5NHNH2 D) NaHCO3/H2O E) Ag(NH3)2+
can you please help me? im stuck, thanks :)
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Question 18 Which reagent would best serve as the basis for a simple chemical test to distinguish between acetophenone and benzophenone? O A GO3/H2SO4 OB. NaHCO3/H20 o Ag NH3)2 O D.Bra/CC14 O E NaCl (12 in NaOH) Question 5 A compound, C5H 100 reacts with phenylhydrazine and gives a positive iodoform test. The compound could be which of these? ОА O OB. CACAČCA Cho CHACHECHICHTE CH,CHCHICO CHI ОС. OD...
which of the following reagents might serve as the basis for a
simple chemical test that would distinguish between 2-butane and
2-butanol ?
Is IR considered "simple"
4 d. 5 e. 6 22. Whic h of the following reagents might serve as the basis for a simple chemical test that would distinguish between 2-Butene and 2-Butanol? a. CrO3 in H2SO0A4 es b. I.R. spectrum Yes d. e. two of the above all of the above
could you please help me with these questions. thank you so much
20. Which reagent would best serve as the basis for a simple chemical test to distinguish between 0 0 CH3CH2CC2C3 and CH3CH2CH2CCH3 a. NaOI (I in NaOH) b. Br CCL c. CrO,/H SO d. NaHCO,/H20 21. Which proton in the following molecule is the most acidic? A) 1 B) 2 C) 3 D) 4 E) 5 22. What product is formed in the aldol reaction of propanal? a....
Which of the following reagents might serve as the basis for a
simple chemical test that would distinguish between the compounds
in the picture. Please explain.
Practice Problems 11 and12-2 IC bility Mode Ward PLE HOME INSERT DESIGN PAGE LAYOUT Karen Herrera Garcia REFERENCES MAILINGS REVIEW VIEW cut Find Times New Ro 12 A A AaBbC AaBbC I AaBbC AaBboc AaBbccD AaBbccDo AaBbccC Rep EE Copy Past B I U x, xa A A EEE E Heading 1 Heading 2...
which
of the two options A or B would produce the compound above?
GH + 2 ~ OH a) Cold dilute KMnO4 b) Doso 4 2) Na2SO₃
Question 5 0/2 points which of the following reagents would you use as the basis for a simple chemical test that would distinguish between ethylbenzene and styrene? sodium borohydride water NaOH bromine Question 8 0/2 points Predict the structure of the major product for the following reaction. step 1 step 2 Zn, HCI AICI: ou or ou on
I got stuck on these, can you please help me? :)
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Which is the most acidic hydrogen in the compound shown? CEN TV 1 O A. III OB. V C. IV D.11 E. Question 18 Which reagent would best serve as the basis for a simple chemical test to distinguish between acetophenone and benzophenone? O A GO3/H2SO4 OB. NaHCO3/H20 o Ag NH3)2 O D.Bra/CC14 O E NaCl (12 in NaOH) Question 5 A compound, C5H 100 reacts...
Determine the yield limiting reagent and the theoretical yield for the following multistep synthesis from the reaction of ethyl acetoacetate. Draw the chemical complete chemical reaction and mechanism of Product B (4,4-diphenyl-3-buten-2-one) to Product C provided the procedure below. Procedure Step 3 [Product B to Product C] Place the product [B] (4,4-diphenyl-3-buten-2-one) from the previous step (3 g) in a 250 ml round bottomed flask, add acetone (40 ml) and 1 M HCl (6 ml). Reflux on a water...
Shown below on Fischer projections are two enantiomeric alcohols. What alkene and what reagents would yield these alcohols upon reacting with each other? Complete the alkene template below to show the structure of the alkene and provide the required reagent(s) by writing it/them above/below the reaction arrow. CH3 CH3 D -OH HO -D X + H -CH2CH3 H3CH2C- CH3 Н. CH2CH2CH3 CH2CH2CH3