Organic Chemistry, Binder Ready Version
2nd Edition
ISBN: 9781118454312
Author: David R. Klein
Publisher: WILEY
expand_more
expand_more
format_list_bulleted
Question
Chapter 1, Problem 77CP
Interpretation Introduction
Interpretation:
To draw pictures showing how the guest (1,2) may bind in the pores of each
Concept introduction:
The binding of guest and host may be simply due to hydrogen bonding or by forming a covalent bond also. The binding of guest and host depends upon the groups present in the respective compounds. If the guest and host has only hydrogen acceptors and hydrogen donor groups then the interaction between these two will be due to hydrogen bonding.
To draw: To draw pictures depicting the binding of guest (1,2) with polymer (A,B) and to propose an explanation for the binding specificity.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Can you explain how I get these here and show the steps plz?
Give the IUPAC name for this compound Hydrocarbon Condensed Formulas
Hint C2H5 CH2CH3 expand that in all the formula
Part A: (CH3)2CHCH(C2H5)CH2CH2CH3
Give the IUPAC name for this compound.
Part B: CH2=C(C2H5)CH2CH2CH3
Give the IUPAC name for this compound.
Part C: (CH3)2C=CHC(C2H5)=CH2
Give the IUPAC name for this compound.
Part D: CH3C=CCH(C2H5)2
Give the IUPAC name for this compound.
Part E: (CH3)3CC=CCH2CH=C(CH3)2
Select/ Match the correct letter from the image below for the IUPAC names given below:
A
B
C
D
3
E
F
G
H
K
L
Part 1. 4-methylheptane
For example.mmmm Answer Letter H _for part 1
Part 2. 2,4-dimethylhexane
Part 3. 2,3-dimethylpentane
Part 4. 2,2-dimethylhexane
Part 5. 2-ethyl-1,1,3,3-tetramethylcyclopentane
Part 6. 3-ethyl-2-methylpentane
Chapter 1 Solutions
Organic Chemistry, Binder Ready Version
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
Knowledge Booster
Similar questions
- Can u show the process as to how to get these?arrow_forwardSketch the expected 'H NMR spectra for the following compound. Label all of the H's in the structure and the corresponding signal for the spectra you sketch. Make sure you include the integration value and the splitting pattern for each signal Indicate how many signals you would expect in the 13C NMRarrow_forwardUse IUPAC naming rules to name the following hydrocarbon compounds: CH2-CH3 | a) CH-CH-CH2-CH-CH-CH3 b) | CH2 CH3 | CH3 CH3 \ / C=C H 1 H CH2-CH3 c) d) CH=C-CH3 e) CH3-CH2-CH2-CH=CH-CH3 f) CH2=CH-CH2-CH=CH-CH3 g) CH3-CH2-C = C-CH2-CH3 h)arrow_forward
- Q5 Name the following : a. b. C. d. e.arrow_forward25. Predict the major product of the following reaction. 1 equivalent of each of the starting materials was used. H₂C CH3 CH3 H3C H3C H3C. CH2 + H3C. heat CH3 CH H.C. CH3 H.C H.C CH3 CH CH3 CH3 A B C Earrow_forwardFind chemical structures based on the below information. a) Chemical formula C6H8O Compound is aromatic plus has two 1H NMR peaks that integrated for 3 each that are singlets (it could have more peaks in the 1H NMR b) Chemical Formula: C6H100 Compounds is conjugated 'H NMR has a signal that integrates for 6 and is a doublet IR spectra has a signal at 1730 cm-1arrow_forward
- Jaslev Propose a synthesis of the following starting from benzene and any other reagents and chemicals. No mechanisms are required. Indicate the condition for each step plus the major product for each step. More than two steps are required. Step 1 Step 2 مہد Brarrow_forwardPart C: The line formula for another branched alkane is shown below. i. In the IUPAC system what is the root or base name of this compound? ii. How many alkyl substituents are attached to the longest chain? iii. Give the IUPAC name for this compound.arrow_forwardPart D: Draw the Structural Formula for 4-ethyl-2-methylhexane Part E. Draw the Structural Formula for 1-chloro-3,3-diethylpentane (Chloro = Cl)arrow_forward
- Part B: The line formula for a branched alkane is shown below. a. What is the molecular formula of this compound? Number of C. Number of H b. How many carbon atoms are in the longest chain? c. How many alkyl substituents are attached to this chain?arrow_forward24. What is the major product for the following reaction? Mg J. H.C CH H,C- Then H₂O OH Br C HO E HO H.C CH H.C- CH₂ CH₂ All of these are possiblearrow_forwardstructures. Explain why the major product(s) are formed over the minor product(s) using the Draw the major and product and the complete mechanism for all products with all resonance mechanism/resonance structures of the major and minor products in your explanation. HONO2 H2SO4arrow_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 Learning
ChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill Education
Principles 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 Education
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Elementary 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