Pescribe what the purpose of ma King_a"derivative" like a semicarbizides, phenyhydrazinDNP solid. How is this helplulur unknowns(s).your

There are hundreds of aldehydes and ketones. For example, HCHO, CH3CHO etc aldehydes and Acetone,…

Answered: Pescribe what the "derivative" like a…

Fundamentals Of Analytical Chemistry

9th Edition

ISBN:9781285640686

Author:Skoog

Publisher:Skoog

Chapter16: Applications Of Neutralization Titrations

Section: Chapter Questions

Problem 16.6QAP

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Hello could somone please help me understand this question
Please help explain 37 & 38
[33] PLEASE HELP
a. + CH3MGBR
c only
I need help part E to part F
Question 5 of 50 -/1 > View Policies Current Attempt in Progress When (S)-2-bromopropanoic acid [(S)-CH3CHBPCO,H] reacts with concentrated sodium hydroxide, the product formed (after acidification) is (R)-2-hydroxypropanoic acid [(R)-CH3CHOHCO2H, commonly known as (R)-lactic acid). This is, of course, the normal stereochemical result for an SN2 reaction. However, when the same reaction is carried out with a low concentration of hydroxide ion in the presence of Ag,0 (where Ag* acts as a Lewis acid), it takes place with overall retention of configuration to produce (S)-2- hydroxypropanoic acid. The mechanism of this reaction involves a phenomenon called neighboring-group participation. Explain why there is a net retention of configuration when Ag* and a low concentration of hydroxide are used. The reaction is a two step process. The missing product produced by step 1 is: (Use single up and single down wedges to show the stereochemistry at the chiral center.) Step I Ag+ H Br CH,
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TO 23 #F ** ## 4 .. ||| V Classify each of the molecules below. A B 4 CH3C=C NH₂2 primary amine Osecondary amine O tertiary amine Explanation G Identifying prinary, secondary, and tertiary amines A $ W S not an amine at all MB 4 # @ #D S P D MA C D *** # D # R # *40 O M PRE 6 19 # . PP G 4 CO @ 25 * 4 10 10 # ♥ a # B sh • Check B B => R W # B RS 9 Ra 00 • a B # S 66 D W W PR ** 19 S # 4 4 BA M @ D #** 4 68 # $ D → * ** @ 48 4 9 S B S a #4 NG D B 55 # 46 3 S 62 4 TO 0 # # 9 4 D B 6 19 4 C 99 6 O primary amine O secondary amine O tertiary amine O not an amine at all P C B . 10 S 4 4 * 4 CH3 —CH=CH—NH2 S ## S 9 B B D Ⓡ 46 9 12 . O 16 S W 4 D # a 0 W #4 D D 1 @ 4 d ♥ 30. D # @ a S 12 #D $ B ** * B D S B 00 # 99 * W e A W 1 W S 9 A D * s @ 10 6 66 19 S P P 14 * 0 a 4 A 16 糖 U a V # # A ** DO E C 24 SP ** N $ B a **** @G S D # 4 S -A W C NE # SOP * ## @A 44 • B S * 15 B $ L ** * # W A Or C D # ** 4. $ A 68 B ** $3 RE B O 6 C $ * O * # @@ #D De A 16 8 W N #0 3 @a *** W 慈 B 4 G # ▶ 10 4 BO $…
Whats the product?
Complete the following reactions. Thank you!
E. What is the correct IUPAC name for the following compound? (- H. N. `CH3 O A. N-benzyl-N-methylamine O B. N-phenyl-N-methylamine O C. 2-amino-1-methyl-2-phenylpropane O D. 1,1-dimethylaniline

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Pescribe what the "derivative" like a semicarbizides DNP solid. How is this helpful in dentify unknowns(s)? of making a , phenyhydraz purpose Dr your