Homework Ch 22 - Reactions of Benzene and Its Derivatives_ Organic Chemistry_ 2023FA-CHEM-012B-201
.pdf
keyboard_arrow_up
School
San Jose City College *
*We aren’t endorsed by this school
Course
012
Subject
Chemistry
Date
May 10, 2024
Type
Pages
29
Uploaded by thanhvotan1 on coursehero.com
9/22/23, 9:58 AM
Chapter 22 - Reactions of Benzene and Its Derivatives: Organic Chemistry: 2023FA-CHEM-012B-201
https://sjeccd.instructure.com/courses/39764/quizzes/250432
1/29
*
Some questions not yet graded
Chapter 22 - Reactions of Benzene and Its Derivatives
Due
Sep 24 at 11:59pm
Points
50
Questions
50
Available
Aug 28 at 12am - Dec 3 at 11:59pm
Time Limit
None
Allowed Attempts
2
Instructions
Attempt History
Attempt
Time
Score
LATEST
Attempt 1
81 minutes
43.8 out of 50 *
Instructions:
1. You have two attempts for this assignment. Canvas will keep the highest score.
2. You should take screenshots of all the questions (and answers) after each attempt. You are only
allowed to see the questions and answers ONCE (after each attempt).
3. You are only allowed to see your score ONCE after each attempt. You cannot see the answers to
questions that are marked incorrectly. You can only see which questions are marked wrong.
4. This assignment may contain some embedded images. If you cannot see the images. it is most likely
because you are using an Apple, Mac, or iPad. Canvas is designed to be compatible with Google
Chrome. Do not use Safari. If you have an Apple, Mac, or iPad, try installing Google Chrome and
using that browser (not Safari). Also. try moving your mouse cursor over the "missing" images. Then, "right click" with your mouse. Then, select "View", "Download", or "Save As". Many students
said that would work.
5. If the due date has already past for this assignment, you are still allowed to go ahead and do the
assignment. Just know that you are allowed to be late for only TWO Homework assignments for the
entire semester. So, you can submit TWO late Homework assignments without any late penalty. After TWO late homework assignments, all other late Homework assignments will receive a ZERO.
The very last date to submit late Homework assignments (up to two late assignments only) is
December 3, 2023 (11:59 PM).
Take the Quiz Again
9/22/23, 9:58 AM
Chapter 22 - Reactions of Benzene and Its Derivatives: Organic Chemistry: 2023FA-CHEM-012B-201
https://sjeccd.instructure.com/courses/39764/quizzes/250432
2/29
Correct answers are hidden.
Score for this attempt: 43.8
out of 50 *
Submitted Sep 22 at 9:55am
This attempt took 81 minutes.
1 / 1 pts
Question 1
What is the major organic product obtained from the following reaction?
3
4
1
2
1 / 1 pts
Question 2
What is the major organic product obtained from the following reaction?
9/22/23, 9:58 AM
Chapter 22 - Reactions of Benzene and Its Derivatives: Organic Chemistry: 2023FA-CHEM-012B-201
https://sjeccd.instructure.com/courses/39764/quizzes/250432
3/29
3
4
2
1
1 / 1 pts
Question 3
What is the major organic product obtained from the following reaction?
4
2
3
1
1 / 1 pts
Question 4
What is the major organic product obtained from the following reaction?
9/22/23, 9:58 AM
Chapter 22 - Reactions of Benzene and Its Derivatives: Organic Chemistry: 2023FA-CHEM-012B-201
https://sjeccd.instructure.com/courses/39764/quizzes/250432
4/29
4
3
1
2
1 / 1 pts
Question 5
What is the electrophile in the reaction of benzene with a mixture of nitric acid and
sulfuric acid?
benzene
NO
2
+
HONO
NO
+
1 / 1 pts
Question 6
What is the electrophile in the reaction of benzene with acetyl chloride, CH
COCl, and
AlCl ?
3
3
9/22/23, 9:58 AM
Chapter 22 - Reactions of Benzene and Its Derivatives: Organic Chemistry: 2023FA-CHEM-012B-201
https://sjeccd.instructure.com/courses/39764/quizzes/250432
5/29
CH
3
+
CH C
≡
O
3
+
CH CO
3
2
−
benzene
1 / 1 pts
Question 7
What is the role of AlCl
in Friedel Crafts acylations using acid chlorides?
3
electrophile
Lewis acid
nucleophile
base
1 / 1 pts
Question 8
Which of the following undergoes the most rapid sulfonation upon treatment with fuming
sulfuric acid?
nitrobenzene
benzoic acid
benzonitrile
benzene
9/22/23, 9:58 AM
Chapter 22 - Reactions of Benzene and Its Derivatives: Organic Chemistry: 2023FA-CHEM-012B-201
https://sjeccd.instructure.com/courses/39764/quizzes/250432
6/29
1 / 1 pts
Question 9
Which of the following undergoes the most rapid acylation upon treatment with acetyl
chloride and AlCl
?
3
chlorobenzene
toluene
1,4-dichlorobenzene
benzene
1 / 1 pts
Question 10
Which of the following sets of substituents are all ortho/para
directing in electrophilic
aromatic substitution reactions?
Br, CH
, NO
3
2
CH
, NH
, Br
3
2
Cl, OCH
, COCH
3
3
NO
, COCH
, COOH
2
3
1 / 1 pts
Question 11
Which of the following sets of substituents are all meta
directing in electrophilic aromatic
substitution reactions?
Your preview ends here
Eager to read complete document? Join bartleby learn and gain access to the full version
- Access to all documents
- Unlimited textbook solutions
- 24/7 expert homework help
Related Questions
6)
NH3 +
Nals +
H2
Type of reaction:
Compiled by: 1dddj.rch/2020-2021
Page 3 of 4
7)
H2O+
SO3 >
H2SO4
Type of reaction:
8)
H2SO4 +
NHLOH >
H20 +
(NH4)2SO4
Type of reaction:
arrow_forward
1. For the rearrangement of cyclopropane to propene at 500°C, the following data have been obtained:
[(CH2)3], M
(CH2), CH,CH=CH2
2.98 x10-
5.55 x10-2
1.60 x10-
8.56x10-3
time, min
15.5
31.0
46.5
What is the rate of disappearance of (CH2); over the time period from 0 to 15.5 minutes?
1.
a. 0.00166 M/min
b. 0.00127 M/min
0.00101 M/min
d. 0.000890 M/min
e. 0.000480 M/min
C.
arrow_forward
The propene reaction with OH radical has a reaction rate constant 2.63 * 10-11 cm3/(molecules*s) and the reaction rate constant with O3 is 1.13*10-17 cm3/(molecules*s). Under polluted conditions (OH=1*106 molecules/cm3 and O3=125 ppb), which reaction dominates? (Assume T=30°C)
arrow_forward
09:30
The following presented reaction scheme lead to the synthesis of which major product from-benzene,
assuming separation of products is possible?
so,
1. Na OH
Product
Product
Cl
O HSO4
2. H,0*
FeCl,
O A. Meta-Chlorophenol
O B. para-ChloroSulfenic acid
OC Para-Chlorophenol
O D. Meta-chloroaniline
Add a caption...
> Status (Custom)
arrow_forward
W)
10 Chem101
p.101edu.co
Office Ho...
Post Attendee - Zo..
General Biology - coc
RN Programs
Question 3 of 19
Write a balanced chemical equation based on the following description:
butanoic acid, CsH-COOH(I) burns in air
arrow_forward
Useful Information:
sodium metam: Commercial grade sodium metam is 33% pure sodium metam by weight and has a density of 1.2 g/mL.
Hydrolysis of metam (Methyl isothiocynate) + H2S
Rate constants for hydrolysis for metam (base catalyzed hydrolysis is negligible)
= 300 mol -1 L. sec -1 , = 1 x 10-8 sec-1
Metam also undergoes photolysis to methyl isothiocyanate with a half-life of 1.6 hrs.
Data for Sacramento River
discharge Q = 75,000 L/min
mean depth = 0.30 m
pH = 7.8
mean width = 3.2 m
dispersion coefficient D = 1.6 x 102 m2/min
Assuming the spill acts acts as a single point source. How long does it take for the maximum contaminant concentration to get to Lake Shasta?
If Na+ acts as conservative (i.e., it is not transformed) tracer, calculate the maximum concentration (in g/L) at Lake Shasta. (Hint: remember that sodium only constitutes a…
arrow_forward
Cambridge International AS Level Chemistry
ot boe slo plgmes s al snsdismonooli
End-of-chapter questions
1 1-bromobutane will undergo reactions when heated, as shown by reactions A and B. ot
dwab on s bl
auoltse s boaub svsd 20 swoll
gab ods-suai la
yel snoso sdr ssiganm
n2 monl gnivims noiteibar VU luad
CH;CH,CH,CH,Br
B
CH;CH,CH,CH,OH
CH;CH,CH=CH, 90u S1s 2O1D Isdh tuo
gomia sli ni qu dgid tod a
guch pecoue
For reactions A and B give the reagents used in each case.
b Reaction A was repeated using 1-iodobutane instead of 1-bromobutane. Explain any difference in the
rate of reaction observed.
p bas-
od mon
c What type of organic reaction is A?
d Show the mechanism for reaction A.
e Reaction A was repeated with 2-bromo-2-methylpropane instead of 1-bromobutane.
i Name the organic compound formed.
elle ii The mechanism of the reaction with 2-bromo-2-methylpropane differs from the mechanism of
smitas nosd asd i anol
reaction A. Describe how the mechanisms differ.
f What type of reaction is…
arrow_forward
08:32 A ¢
READ-ONLY - This is an older file format. T..
1
Part II
Q1. Complete any three of the following reactions with mechanism.
CH-CH-CH3-CH;
i)
KMno,
Heat
NABH,
NaOH
iii)
2
NH,-X
iv)
II
%3D
arrow_forward
ORGANIC CHEMISTRY - PERICYCLIC REACTIONS
Indicate the products, no need to design the mechanisms.
arrow_forward
4)
Complete given reactions. (They have missing parts)
Categorize them accerding to their forbidden degrees
and
write their type of passing
(0*) >
42
22
->
49
50
Hel )
3
3
c)
->
2
76
76
Se lo7)
->
34
(P
35
arrow_forward
Pericyclic Reactions: Convert 1a to 1b
Indicate what type of reactions and mechanisms occured in each step. Indicate reagents/conditions.
arrow_forward
01:50
4G
File Details
4CH003/UM1: Fundamentals of...
Introduction
NaBH4
OH
C=0
H
benzophenone
diphenylmethanol
Ketones are readily reduced to secondary alcohols by reaction with sodium
borohydride. The aim of this experiment is to determine the time required to
effect
the complete conversion
of the ketone, benzophenone to
diphenylmethanol at room temperature. This investigation may be achieved
by isolating and analyzing the reaction product after different reduction times.
Infrared spectroscopy affords a convenient method of analysis; by comparing
the IR spectrum of the crude reaction product at different time intervals one
would expect to see the intensity of the hydroxyl absorption peak increase
relative to that of the original carbonyl peak. From this you can deduce the
optimum time for the reduction process at room temperature.
Procedure
Note the "reduction time" that the demonstrator assigns to your group.
Different groups will be assigned different times, eithert = 2.5 minutes,…
arrow_forward
9:52 PM Tue May 10
88
HW6-2 -
HW6-2
203+HE+5+Key
3. Which of these two reactions would go better? Why?
HOCH3
CH3CH2CH2CI
CHCH,CH20CH3
NaOCH3
CH3CH2CH2CI
CH3CH2CH2OCH3
arrow_forward
Sunday 7/2 X
O https://learn.ejust.org/first/mod/quiz/attempt.php?attempt=D453621&cmid%3874208&p=
JUSTLearn First Semester 2021
English (en) -
The major product from the reaction of H2O with propene in the presence of acid catalyst is:-
O 1,3-propanediol
O 2-propanol
O 1-propanol
O 1,2-propanediol
O propanal
Which of the following does not produce silver mirror when reacts with Tollen's reagent?
O Butanone
ut of
O Benzaldehyde
uestion
O butanal
O Formaldehyde
O heptanal
Type here to search
1O
* 10
144
#3
3
@
$
4.
5.
&
7
V
8.
E
R
Y
S
F
G
H
J
K
%3D
+ 1
arrow_forward
arrow_forward
A synthon is a concept in retrosynthetic analysis. It is defined as a structural unit within a
molecule which is related to a possible synthetic operation.
Example:
OH
bond breaks here
synthesis
Br
+
retrosynthesis
NEC Na -NaBr
Synthons
C-C bond formation
synthetic equivalents
Br
D=00
CN
OH
||
ⒸC=N
H₂O, H+
hydrolysis
do not exist
exist
functional group transformation
Common synthons:
C1 synthons: carbon dioxide, carbon monoxide, cyanide, formaldehyde C2
synthons: acetylene, acetaldehyde
C₂H4OH synthon: ethylene oxide
OH
Carbocation synthons: alkyl halides, carbonyl C
Carbanion synthons: Grignard reagents, organolithiums, malonic ester/acetoacetic ester, terminal
alkyne
Use the synthons listed above, propose how you would synthesis the following molecules:
arrow_forward
didentify
the
Allowry
reactions, as
substitution,
elimination, or addition DrawWelection arrows to show how the
in each reactors Circle and identify any reactive
bands break & form
intermediates of carbon.
Ħ
Br
Br
→ AH-Br →→ → XB²
arrow_forward
Macmillanne Bed
Chapter 86
Question 7 of 14
View Policies
Current Attempt in Progress
eTextbook and Media
Identify reagents that can be used to achieve the following transformation:
Save for Later
How To Write Biolo...
O 1) NaOH, 2) RCO3H, 3) H3O+
O 1) Conc. H₂SO4, heat, 2) RCO³H, 3) H³O*
O 1) Conc. H₂SO4, heat, 2) OsO4, NMO
O 1) NaOEt, 2) OsO4, NMO
>
F1
F2
Type here to search
OH
OH
8- &
▶/11
a Amazon.com 150 E...
F3
F4
04
F5
OH
Attempts: C
F6
PrtSc
arrow_forward
10. What is the major organic product generated in the reaction below?
HO
HO
40||!!!!!!
(A)
OH
......
(B)
1) 03
2) (CH3)2S
HO
O
(C)
H
НО.
(D)
arrow_forward
The following figure shows the energy profile of a nucleophilic substitution reaction.
Potential energy
:ÖH
H
HII.C
H
C-1
H
HO--C---I
HH
Reaction coordinate
H
-CH
HO–CHITH
H
+ 1
According to this, it is correct to affirm:
O The activation energy (4G°) shows that it is thermodynamically favorable.
O Represents a reaction that occurs in one step where a pentavalent chemical species is
formed.
O The intermediate has lower energy than any transition state.
O The formation of the intermediate releases energy and is therefore thermodynamically
favourable.
arrow_forward
The reaction of ozone
with 2-butene leads to -10
formation of aldehyde + O
ketones, aldehyde + alcohol,
two molecules of carboxylic
acid O.
arrow_forward
Student Instructions:
In this assignment titled "electrophilic addition reactions" you should fill the empty cells by either
giving the formula of the necessary reactants to obtain a specific product or the formula of
possible products give the reactant. This is a activity and should be handed in by the
date indicated in the course calendar.
Reactants formulas
CH3
+
HCI
Products formulas
H3C-O
D
H3C-07
CHCH=CH-CH3 +H3C-HC-
Rr
Br
arrow_forward
please help!
nererences to access important values if needed for this question.
Complete the equation for the following reaction by drawing a structural formula for the missing organic product.
CH3CH,NH,
(CH₂)₂COOH
3
0-
. You do not have to consider stereochemistry.
• You do not have to explicitly draw H atoms.
• Draw cations and anions in separate sketchers.
-/
5
88
H₂O
ChemDoodle
0-
15424
000- / [F
?
Show Transcribed Text
G
Draw a structural formula for the missing product in the following reaction.
CH₂CH₂CHE OH + NaHCO3 H₂0
CH₂CH₂
? + CO2 + H2O
• You do not have to consider stereochemistry.
You do not have to explicitly draw H atoms.
• Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher.
✓✓8)
24
///.000. F
Ⓡ
arrow_forward
Write down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed:
CH,-0
CH₂
0
Separate each name with a comma. You will find useful information in the ALEKS Data resource.
Ethanol, Methanol, Water
a Y
arrow_forward
Mastering Chemistry: 1212 - Ch 1 x
ringchemistry.com/myct/itemView?assignmentProblemID=135892233
CHEM 1212 Spring 2020
Joyce
<1212 Ch 14 B
Problem 14.30 -Enhanced - with Feedback
I Review | Constants | Per
Consider the following reaction:
2NO(g) + 2H2(g)→N2(g) +2H2O(g).
You may want to reference (Pages 576 - 581) Section 143
while completing this problem.
Part B
If the rate constant for this reaction at 1000 K is 6.0 x 10 M's, what is the reaction rate when NOJ = 3.90x10-2M and H2l :
ptann
1.40x10-2 M?
Express your answer using two significant figures.
Vο ΑΣΦ
rate =
0.80
M/s
Submit
Previous Answers Request Answer
X Incorrect; Try Again; 4 attempts remaining
Part C
Type here to search
5:58 F
2/24/2
hp
II
arrow_forward
A.
B.
C.
D.
E.
F.
G.
1²
C6H1002
NaOH/H₂O
1) R₂BH
2) H₂O2, H₂O, NaOH
Br₂ 1 eq
120 °C
1) NaH
2) EtI
3) Poison Catalyst
/H₂
4) 03, -78°C; Zn
H
HO OH
arrow_forward
Brown, Intro Orgaic Chemistry, be
Hep System Announcements
Question 7
Draw the structural formula for a cycloalkene of molecular formula CHn that reacts with Cl, to give the following compound:
CI
Cl
Edit
By accessing this Question Assistance, you will learn while you earn points based on the Point Potential Policy set by your instructor.
arrow_forward
ugen.wileyplus.com/edugen/student/
aintr.uni
Klein, Organic Chemistry, 3e
actice
Assignment
Gradebook
ORION
Downloadable eTextbook
gnment
Give the major organic product of the following reaction.
:O + HN
(CH3)2CHI
H30+
?
heat
OH
y.
arrow_forward
V a reaction in which all bond-breaking and bond-forming occurs at the same time
a reaction in which bond forming occurs first
O a substitution reaction
QUESTION 28
Which of the fallowing is the rate equation for the following SN2 reaction?
CN
Br
NaCN
+ NaBr
O Rate = kl1-bromopropane]
O Rate = kINaCN)
Rate = k1-bromopropane] [NACN]
Rate = k[1-bromopropane]2
O Rate = k[1-bromopropane]2 [NACNJ2
QUESTION 29
Save All Answer
Tlick Saveand Submit to save and submit. Click Save All Answers to save all answers.
arrow_forward
pluginfile.php/477064/modresource/content/0/Chem%20154%20Exam%202%20F2019%20Loudon%20ch%204.pdf
ch 4.pdf
3/5
5.1
Mechanisms. Using curved arrows, suggest a reasonable mechanism for
each indicated reaction.
H3PO4
water, dilute
a)
b)
H3PO4
HO.
H20
arrow_forward
Describe the reaction to form the catalyst L-prolinamide. (reaction is added below)
.
arrow_forward
←
A
→ C
FI
4
app.aktiv.com
@
F2
(CH3CH₂)ǝN
OH
80
F3
3 S PP
Br
U
000
000
F4
in
FS
S
Problem 23 of 55
MacBook Air
F6
g
F7
A
B
с
D
E
3 C
NaH
DMF
NaCl
DMF
NaHCO3
DMF
NaH
H₂O
PP.
(CH3CH₂)2N
DII
F8
O
Done
DD
FO
PP
S
PS
A
F10
P 4
8 AX
B
U
F11
★
+
0
Submit
(1))
⠀
F12
arrow_forward
Predict the product of the following organic reaction:
CH₂
CH
O
||
C–CH2–CH=CH—(CH2)3 CH3
(CH₂)3 CH=CH- - CH₂
CH3
+ 4 H₂
Ni
CH,−O -C–CH2–CH=CH–CH=CH–CH2–CH3
Specifically, in the drawing area below, draw the chemical structure of the product P. If there is no product, because this reaction won't happen, check the No
reaction box under the drawing area.
Click and drag to start drawing a structure.
×
Ś
+
arrow_forward
SEE MORE QUESTIONS
Recommended textbooks for you
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY
Related Questions
- 6) NH3 + Nals + H2 Type of reaction: Compiled by: 1dddj.rch/2020-2021 Page 3 of 4 7) H2O+ SO3 > H2SO4 Type of reaction: 8) H2SO4 + NHLOH > H20 + (NH4)2SO4 Type of reaction:arrow_forward1. For the rearrangement of cyclopropane to propene at 500°C, the following data have been obtained: [(CH2)3], M (CH2), CH,CH=CH2 2.98 x10- 5.55 x10-2 1.60 x10- 8.56x10-3 time, min 15.5 31.0 46.5 What is the rate of disappearance of (CH2); over the time period from 0 to 15.5 minutes? 1. a. 0.00166 M/min b. 0.00127 M/min 0.00101 M/min d. 0.000890 M/min e. 0.000480 M/min C.arrow_forwardThe propene reaction with OH radical has a reaction rate constant 2.63 * 10-11 cm3/(molecules*s) and the reaction rate constant with O3 is 1.13*10-17 cm3/(molecules*s). Under polluted conditions (OH=1*106 molecules/cm3 and O3=125 ppb), which reaction dominates? (Assume T=30°C)arrow_forward
- 09:30 The following presented reaction scheme lead to the synthesis of which major product from-benzene, assuming separation of products is possible? so, 1. Na OH Product Product Cl O HSO4 2. H,0* FeCl, O A. Meta-Chlorophenol O B. para-ChloroSulfenic acid OC Para-Chlorophenol O D. Meta-chloroaniline Add a caption... > Status (Custom)arrow_forwardW) 10 Chem101 p.101edu.co Office Ho... Post Attendee - Zo.. General Biology - coc RN Programs Question 3 of 19 Write a balanced chemical equation based on the following description: butanoic acid, CsH-COOH(I) burns in airarrow_forwardUseful Information: sodium metam: Commercial grade sodium metam is 33% pure sodium metam by weight and has a density of 1.2 g/mL. Hydrolysis of metam (Methyl isothiocynate) + H2S Rate constants for hydrolysis for metam (base catalyzed hydrolysis is negligible) = 300 mol -1 L. sec -1 , = 1 x 10-8 sec-1 Metam also undergoes photolysis to methyl isothiocyanate with a half-life of 1.6 hrs. Data for Sacramento River discharge Q = 75,000 L/min mean depth = 0.30 m pH = 7.8 mean width = 3.2 m dispersion coefficient D = 1.6 x 102 m2/min Assuming the spill acts acts as a single point source. How long does it take for the maximum contaminant concentration to get to Lake Shasta? If Na+ acts as conservative (i.e., it is not transformed) tracer, calculate the maximum concentration (in g/L) at Lake Shasta. (Hint: remember that sodium only constitutes a…arrow_forward
- Cambridge International AS Level Chemistry ot boe slo plgmes s al snsdismonooli End-of-chapter questions 1 1-bromobutane will undergo reactions when heated, as shown by reactions A and B. ot dwab on s bl auoltse s boaub svsd 20 swoll gab ods-suai la yel snoso sdr ssiganm n2 monl gnivims noiteibar VU luad CH;CH,CH,CH,Br B CH;CH,CH,CH,OH CH;CH,CH=CH, 90u S1s 2O1D Isdh tuo gomia sli ni qu dgid tod a guch pecoue For reactions A and B give the reagents used in each case. b Reaction A was repeated using 1-iodobutane instead of 1-bromobutane. Explain any difference in the rate of reaction observed. p bas- od mon c What type of organic reaction is A? d Show the mechanism for reaction A. e Reaction A was repeated with 2-bromo-2-methylpropane instead of 1-bromobutane. i Name the organic compound formed. elle ii The mechanism of the reaction with 2-bromo-2-methylpropane differs from the mechanism of smitas nosd asd i anol reaction A. Describe how the mechanisms differ. f What type of reaction is…arrow_forward08:32 A ¢ READ-ONLY - This is an older file format. T.. 1 Part II Q1. Complete any three of the following reactions with mechanism. CH-CH-CH3-CH; i) KMno, Heat NABH, NaOH iii) 2 NH,-X iv) II %3Darrow_forwardORGANIC CHEMISTRY - PERICYCLIC REACTIONS Indicate the products, no need to design the mechanisms.arrow_forward
- 4) Complete given reactions. (They have missing parts) Categorize them accerding to their forbidden degrees and write their type of passing (0*) > 42 22 -> 49 50 Hel ) 3 3 c) -> 2 76 76 Se lo7) -> 34 (P 35arrow_forwardPericyclic Reactions: Convert 1a to 1b Indicate what type of reactions and mechanisms occured in each step. Indicate reagents/conditions.arrow_forward01:50 4G File Details 4CH003/UM1: Fundamentals of... Introduction NaBH4 OH C=0 H benzophenone diphenylmethanol Ketones are readily reduced to secondary alcohols by reaction with sodium borohydride. The aim of this experiment is to determine the time required to effect the complete conversion of the ketone, benzophenone to diphenylmethanol at room temperature. This investigation may be achieved by isolating and analyzing the reaction product after different reduction times. Infrared spectroscopy affords a convenient method of analysis; by comparing the IR spectrum of the crude reaction product at different time intervals one would expect to see the intensity of the hydroxyl absorption peak increase relative to that of the original carbonyl peak. From this you can deduce the optimum time for the reduction process at room temperature. Procedure Note the "reduction time" that the demonstrator assigns to your group. Different groups will be assigned different times, eithert = 2.5 minutes,…arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY