CH12-1Questions_Key
pdf
keyboard_arrow_up
School
Binghamton University *
*We aren’t endorsed by this school
Course
CHEM-531
Subject
Chemistry
Date
Feb 20, 2024
Type
Pages
2
Uploaded by DoctorProton7569
CHEM 332 Spring 2024 Chapter 12-1 Success Hours Key 1.
Draw three additional resonance structures for each of the following species and use proper curved arrow notation to show the interconversion between the structures. Identify the most stable resonance forms. 2.
Challenge: Draw resonance structures for the anion below. Note that the structure below has one additional resonance form compared to the previous examples. 3.
Provide an IUPAC name, using common names, for each of the following molecules. Use ortho, meta, and para
where appropriate.
CHEM 332 Spring 2024 4.
Provide an IUPAC name, without using common names, for each of the following molecules. 5.
State the number of pi-bonding electrons in each species below. 6.
Fill in appropriate reagents and conditions to cause the synthetic transformations shown. 7.
Provide a reasonable synthetic pathway for the transformation shown below:
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 Documents
Related Questions
Draw significant resonance structures for the following compound
Qay
Step 1
First, add curved arrow(s) to show the resonance using the following pattern: an allylic carbocation. Modify the second structure
given to draw the new resonance structure. Include lone pairs and charges in your structure. Use the +and-tools to add charges
to an atom, and use the single bond tool to add/remove double bonds
FODCX000
1+1+1+1
ay ay
-
Hal
0
P
S
Be
1
2
arrow_forward
Organic Chemistry Question
PLEASE SHOW STEP BY STEP, WITH ARROWS! ALSO PLEASE INCLUDE ALL ELECTRON LONE PAIRS AND CHARGES FOR STRUCTURES IF NECESSARY!
arrow_forward
Can you explain it? Provide examples with the various steps and explanations. How halogens affect the boiling/melting point? Does number of halogens affect it? For example, Ch3-Ch3 vs Ch3-Br vs Br-Ch3-Br
arrow_forward
(please reyekson and correct answer )
arrow_forward
Please help with both questions
arrow_forward
Instructions:
Make sure to make your explanations precise and show your complete solutions. Thank you
Draw a labeled molecular diagram to explain how the Law of Mass Conservation applies to the chemical reaction below.
?? + ??? → ? ???
Make sure to label each atom/molecule on the reactant and product side. You may draw arrows to indicate bond formation or zigzag lines to indicate breaking of bonds.
arrow_forward
Curved arrows are used to illustrate the flow of electrons. Using
the provided starting and product structures, draw the curved
electron-pushing arrows for the following reaction or
mechanistic steps.
Be sure to account for all bond-breaking and bond-making
steps.
:OH:
Select to Add Arrows
H₂O
3
H₂
H
HH
H
:Br:Ⓒ
HH
Select to Add Arrows
H₂O
17
:Br:
H
H
Please select a drawing or reagent from the question area
arrow_forward
Use the Reference
What is the IUPAC name of the following compound?
ball & stick
+ labels
-
Submit Answer
Retry Entire Group
9 more group attempts remaining
2reg
arrow_forward
Draw the organic product of the reaction
arrow_forward
Solve please. Should 100% sure of answer.
With some explanation in sentences.
arrow_forward
1. Nucleophile and Electrophile Identification
a. Which of the following species is likely to behave as a
in the box below each species.
electrophile? Put your answer
nucleophile and which as an
CH3O
NH4
NO2
Species
CN
Br
Nuc or Elect?
CH
H-C C-H
НО"
Species
CH3S
NH3
Nuc or Elect?
b. Draw the following Functional Groups, including lone pairs of electrons. Predict the bond polarity of the
functional group using S+ and &- if applicable (think about electronegativity differences!). Then, identify ALL
nucleophilic and electrophilic sites using your knowledge of bond polarity.
EXAMPLE: Alcohol
Aldehyde
Amine
Acid Chloride
Hас-о-н
electrophilic
electrophilic
nucleophilic
Alkene
Ketone
Ether
Carboxylic Acid
arrow_forward
Please correct answer and don't use hand rating
arrow_forward
i need the answer quickly
arrow_forward
Please help me figure out the IUPAC names that come from combining the compounds in the first column (Compounds should match small on right column). Thanks !
arrow_forward
Rank the following active methylene compounds in order of decreasing acid strength.
H₂C
O
CEN
H3C.
O
most acidic
least acidic
Answer Bank
CH3
H3C
NO₂
H3C
O₂N
NO₂
CH3
arrow_forward
please help and draw answer and circle the answer
arrow_forward
Please correct answer and don't use hand raiting
arrow_forward
First, add curved arrow(s) to show the
resonance using the following pattern: an allylic
carbocation. Modify the second structure given
to draw the new resonance structure. Include
lone pairs and charges in your structure. Use
the + and - tools to add charges to an atom, and
use the single bond tool to add/remove double
bonds.
.CH3
.CH3
ČH3
arrow_forward
Use the References to access important values if needed for this question.
Complete the following one-step reaction by writing the IUPAC name of the
reactant.
?
H2S04
CH3CH2CHCOH
CH3
Submit Answer
Retry Entire Group
No more group attempts remain
Previous
Next
Save and Exit
arrow_forward
Please help with all parts i am using this to study
arrow_forward
4:23
Question 10 of 10
Reset
Provide the correct IUPAC name for
the compound shown here.
ОН
Submit
1- 5,5- 3- 5-
1,1- 3,3-
tert- cyclo sec- di tri iso
hex meth eth) pent] but] (acid
oic al ol an oxy yl
Tap here or pull up for additional resources
X
arrow_forward
Current Attempt in Progress
For the given cation, draw all significant resonance forms and rank them from most significant to least significant. Briefly explain the
rankings.
Part 1
Ⓒ
H
Because this is a charged species, let's focus on resonance patterns that can delocalize the charge. First, add curved arrow(s) to
show the resonance using the following pattern: a lone pair next to a carbocation. Modify the second structure given to draw the
new resonance structure. Include relevant formal charges in your structure. Use the + and tools to add/remove charges to an
atom, and use the single bond tool to add/remove double bonds.
Part 2
Edit Drawing
eTextbook and Media
Save for Later
Attempts: 0 of 3 used Submit Answer
arrow_forward
SEE MORE QUESTIONS
Recommended textbooks for you
![Text book image](https://www.bartleby.com/isbn_cover_images/9780618974122/9780618974122_smallCoverImage.gif)
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Related Questions
- Draw significant resonance structures for the following compound Qay Step 1 First, add curved arrow(s) to show the resonance using the following pattern: an allylic carbocation. Modify the second structure given to draw the new resonance structure. Include lone pairs and charges in your structure. Use the +and-tools to add charges to an atom, and use the single bond tool to add/remove double bonds FODCX000 1+1+1+1 ay ay - Hal 0 P S Be 1 2arrow_forwardOrganic Chemistry Question PLEASE SHOW STEP BY STEP, WITH ARROWS! ALSO PLEASE INCLUDE ALL ELECTRON LONE PAIRS AND CHARGES FOR STRUCTURES IF NECESSARY!arrow_forwardCan you explain it? Provide examples with the various steps and explanations. How halogens affect the boiling/melting point? Does number of halogens affect it? For example, Ch3-Ch3 vs Ch3-Br vs Br-Ch3-Brarrow_forward
- (please reyekson and correct answer )arrow_forwardPlease help with both questionsarrow_forwardInstructions: Make sure to make your explanations precise and show your complete solutions. Thank you Draw a labeled molecular diagram to explain how the Law of Mass Conservation applies to the chemical reaction below. ?? + ??? → ? ??? Make sure to label each atom/molecule on the reactant and product side. You may draw arrows to indicate bond formation or zigzag lines to indicate breaking of bonds.arrow_forward
- Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic steps. Be sure to account for all bond-breaking and bond-making steps. :OH: Select to Add Arrows H₂O 3 H₂ H HH H :Br:Ⓒ HH Select to Add Arrows H₂O 17 :Br: H H Please select a drawing or reagent from the question areaarrow_forwardUse the Reference What is the IUPAC name of the following compound? ball & stick + labels - Submit Answer Retry Entire Group 9 more group attempts remaining 2regarrow_forwardDraw the organic product of the reactionarrow_forward
- Solve please. Should 100% sure of answer. With some explanation in sentences.arrow_forward1. Nucleophile and Electrophile Identification a. Which of the following species is likely to behave as a in the box below each species. electrophile? Put your answer nucleophile and which as an CH3O NH4 NO2 Species CN Br Nuc or Elect? CH H-C C-H НО" Species CH3S NH3 Nuc or Elect? b. Draw the following Functional Groups, including lone pairs of electrons. Predict the bond polarity of the functional group using S+ and &- if applicable (think about electronegativity differences!). Then, identify ALL nucleophilic and electrophilic sites using your knowledge of bond polarity. EXAMPLE: Alcohol Aldehyde Amine Acid Chloride Hас-о-н electrophilic electrophilic nucleophilic Alkene Ketone Ether Carboxylic Acidarrow_forwardPlease correct answer and don't use hand ratingarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9780618974122/9780618974122_smallCoverImage.gif)
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning