ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT
2nd Edition
ISBN: 9781119288510
Author: Klein
Publisher: WILEY
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Question
Chapter 1.2, Problem 3ATS
Interpretation Introduction
Interpretation: The constitutional isomer of the given compound has to be drawn by using its molecular formula C3H8O.
Concept introduction: The arrangement of atoms that are bonded together determines its constitution and molecular formula of that particular compound.
This concept is referred as structural isomers or in more modern term constitutional isomers.
Each atom has a typical valency or valence which is defined as the ability of an atom to form a
Oxygen and hydrogen atoms are divalent and monovalent in nature.
To find: The constitutional isomer of the given compound
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Complete the reaction in the drawing area below by adding the major products to the right-hand side.
If there won't be any products, because nothing will happen under these reaction conditions, check the box under the drawing area instead.
Note: if the products contain one or more pairs of enantiomers, don't worry about drawing each enantiomer with dash and wedge bonds. Just draw one molecule
to represent each pair of enantiomers, using line bonds at the chiral center.
+ More...
☐
☐
: ☐
+
G
1. NaOMe
Click and drag to start
drawing a structure.
2. H
+
6. Ammonia reacts with nitrogen monoxide and oxygen to form nitrogen and water vapor. If the
rate of consumption of NO is 4.5 mollitermin)
(a) Find the rate of reaction
(b) Find the rate of formations of N; and HO
(c) Find the rate of consumption of NH, and O
4NH: 4NO 0:4: +60
34. Give the expected major product of each of the following reactions.
Conc. HI
a. CH3CH2CH2OH
b. (CH3)2CHCH2CH2OH
Conc. HBr
H
Conc. HI
C.
OH
Conc.HCI
d. (CH3CH2)3COH
Chapter 1 Solutions
ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT
Ch. 1.2 - Prob. 1LTSCh. 1.2 - Prob. 1PTSCh. 1.2 - Prob. 2ATSCh. 1.2 - Prob. 3ATSCh. 1.2 - Prob. 4ATSCh. 1.3 - Prob. 2LTSCh. 1.3 - Prob. 5PTSCh. 1.3 - Prob. 6ATSCh. 1.3 - Prob. 7ATSCh. 1.3 - Prob. 8ATS
Ch. 1.3 - Prob. 9ATSCh. 1.3 - Prob. 3LTSCh. 1.3 - Prob. 10PTSCh. 1.3 - Prob. 11ATSCh. 1.3 - Prob. 12ATSCh. 1.4 - Prob. 4LTSCh. 1.4 - Prob. 13PTSCh. 1.4 - Prob. 14ATSCh. 1.5 - Prob. 5LTSCh. 1.5 - Prob. 15PTSCh. 1.5 - Prob. 16ATSCh. 1.6 - Prob. 6LTSCh. 1.6 - Prob. 17PTSCh. 1.6 - Prob. 18ATSCh. 1.9 - Prob. 19CCCh. 1.9 - Prob. 20CCCh. 1.9 - Prob. 21CCCh. 1.9 - Prob. 7LTSCh. 1.9 - Prob. 22PTSCh. 1.9 - Prob. 23ATSCh. 1.9 - Prob. 24CCCh. 1.10 - Prob. 8LTSCh. 1.10 - Prob. 25PTSCh. 1.10 - Prob. 26PTSCh. 1.10 - Prob. 27ATSCh. 1.10 - Prob. 28ATSCh. 1.11 - Prob. 9LTSCh. 1.11 - Prob. 29PTSCh. 1.11 - Prob. 30ATSCh. 1.11 - Prob. 31ATSCh. 1.12 - Prob. 10LTSCh. 1.12 - Prob. 32PTSCh. 1.12 - Prob. 33ATSCh. 1 - Prob. 34PPCh. 1 - Prob. 35PPCh. 1 - Prob. 36PPCh. 1 - Prob. 37PPCh. 1 - Prob. 38PPCh. 1 - Prob. 39PPCh. 1 - Prob. 40PPCh. 1 - Prob. 41PPCh. 1 - Prob. 42PPCh. 1 - Prob. 43PPCh. 1 - Prob. 44PPCh. 1 - Prob. 45PPCh. 1 - Prob. 46PPCh. 1 - Prob. 47PPCh. 1 - Prob. 48PPCh. 1 - Prob. 49PPCh. 1 - Prob. 50PPCh. 1 - Prob. 51PPCh. 1 - Prob. 52PPCh. 1 - Prob. 53PPCh. 1 - Prob. 54PPCh. 1 - Prob. 55PPCh. 1 - Prob. 56PPCh. 1 - Prob. 57PPCh. 1 - Prob. 58PPCh. 1 - Prob. 59PPCh. 1 - Prob. 60PPCh. 1 - Prob. 61PPCh. 1 - Prob. 62PPCh. 1 - Prob. 63IPCh. 1 - Prob. 67IPCh. 1 - Prob. 68IPCh. 1 - Prob. 69IPCh. 1 - Prob. 70CPCh. 1 - Prob. 71CPCh. 1 - Prob. 72CPCh. 1 - Prob. 73CPCh. 1 - Prob. 74CPCh. 1 - Prob. 75CPCh. 1 - Prob. 76CPCh. 1 - Prob. 77CP
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Similar questions
- 42. Which of the following halogenated compounds can be used successfully to prepare a Grignard reagent for alcohol synthesis by subsequent reaction with an aldehyde or ketone? Which ones cannot and why? H3C CH3 a. Br H OH b. Cl C. I H H d. Cl e. H OCH3 Br Harrow_forwardFor each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. ? Will the first MgBr product that forms in this reaction create a new CC bond? olo ? OH جمله O Yes Ⓒ No MgCl ? Will the first product that forms in this reaction create a new CC bond? Click and drag to start drawing a structure. Yes No X ☐ : ☐ टे PHarrow_forwardAssign all the protonsarrow_forward
- 9 7 8 C 9 8 200 190 B 5 A -197.72 9 8 7 15 4 3 0: ང་ 200 190 180 147.52 134.98 170 160 150 140 130 120 110 100 90 90 OH 10 4 3 1 2 -143.04 140. 180 170 160 150 140 130 120 110 100 90 CI 3 5 1 2 141.89 140.07 200 190 180 170 160 150 140 130 120 110 100 ៖- 90 129. 126.25 80 70 60 -60 50 40 10 125.19 -129.21 80 70 3.0 20 20 -8 60 50 10 ppm -20 40 128.31 80 80 70 60 50 40 40 -70.27 3.0 20 10 ppm 00˚0-- 77.17 30 20 20 -45.36 10 ppm -0.00 26.48 22.32 ―30.10 ―-0.00arrow_forwardAssign all the carbonsarrow_forwardC 5 4 3 CI 2 the Righ B A 5 4 3 The Lich. OH 10 4 5 3 1 LOOP- -147.52 T 77.17 -45.36 200 190 180 170 160 150 140 130 120 110 100 90 80 70 60 50 40 30 20 10 ppm B -126.25 77.03 200 190 180 170 160 150 140 130 120 110 100 90 80 70 60 50 40 30 20 10 ppm 200 190 180 170 160 150 140 130 120 110 100 90 80 TO LL <-50.00 70 60 50 40 30 20 10 ppm 45.06 30.18 -26.45 22.36 --0.00 45.07 7.5 1.93 2.05 -30.24 -22.36 C A 7 8 5 ° 4 3 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 ppm 9 8 5 4 3 ཡི་ OH 10 2 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 5 4 3 2 that th 7 I 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 115 2.21 4.00 1.0 ppm 6.96 2.76 5.01 1.0 ppm 6.30 1.00arrow_forward
- Curved arrows were used to generate the significant resonance structure and labeled the most significant contribute. What are the errors in these resonance mechanisms. Draw out the correct resonance mechanisms with an brief explanation.arrow_forwardWhat are the: нсе * Moles of Hice while given: a) 10.0 ml 2.7M ? 6) 10.ome 12M ?arrow_forwardYou are asked to use curved arrows to generate the significant resonance structures for the following series of compounds and to label the most significant contributor. Identify the errors that would occur if you do not expand the Lewis structures or double-check the mechanisms. Also provide the correct answers.arrow_forward
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