Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN: 9780618974122
Author: Andrei Straumanis
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 6, Problem 2CTQ
(a)
Interpretation Introduction
Interpretation:
The explanation for name eclipsed and staggered should be given.
Concept Introduction:
The spatial arrangement of atoms in a molecule obtained by rotation around carbon - carbon single bond is known as conformation.
(b)
Interpretation Introduction
Interpretation:
The explanation for favorability of staggered conformation over eclipsed conformation should be given.
Concept Introduction:
The spatial arrangement of atoms in a molecule obtained by rotation around carbon - carbon single bond is known as conformation.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
a. Which is more stable; cis-1,3-dimethylcyclohexane or trans-1,3-
dimethylcyclohexane?
i. Draw chair configuration of cis-1,3-dimthylcyclohexane and its alternate
chair. conformation shown above.
ii. Of the two chair conformation, which is more stable? Explain:.
iii. Draw chair configuration of trans-1,3-dimethylcyclohexane and its
alternate chair, conformation shown above.
iv. Of the two chair conformation, which is more stable? Explain.
v. Which is more stable overall, cis or trans form?
An explanation would really help,
Imagine that this worksheet has sucked you the plane of the page, and you are now facing the indicated bond of the drawn molecule.
a. Draw the six main Newman projections for the indicated bond: three eclipsed, three staggered.
b. Label which conformers are eclipsed ands taggered.c. Identify the most and least stable conformer, and explain your reasoning.
Chapter 6 Solutions
Organic Chemistry: A Guided Inquiry
Ch. 6 - Prob. 1CTQCh. 6 - Prob. 2CTQCh. 6 - Prob. 4CTQCh. 6 - Prob. 5CTQCh. 6 - Complete this graph of relative potential energy...Ch. 6 - Prob. 7CTQCh. 6 - Prob. 8CTQCh. 6 - Prob. 9CTQCh. 6 - Consider the Newman projection below. a. Draw a...Ch. 6 - Draw a Newman projection showing the lowest P.E....
Ch. 6 - Prob. 12CTQCh. 6 - Prob. 13CTQCh. 6 - In skeletal representations the hydrogens are not...Ch. 6 - Prob. 15CTQCh. 6 - Prob. 16CTQCh. 6 - Prob. 17CTQCh. 6 - Prob. 19CTQCh. 6 - Prob. 20CTQCh. 6 - Prob. 21CTQCh. 6 - Prob. 22CTQCh. 6 - Prob. 23CTQCh. 6 - Draw a constitutional isomer of pentane,...Ch. 6 - How many H’s are lost from the molecular formula...Ch. 6 - How many ifs are lost from the molecular formula...Ch. 6 - Prob. 27CTQCh. 6 - What is the degree of unsaturation for the example...Ch. 6 - Without counting hydrogens, determine which one of...Ch. 6 - Determine the degree of unsaturation (and draw a...Ch. 6 - a model of each molecule shown above: Is the...Ch. 6 - Prob. 32CTQCh. 6 - Prob. 33CTQCh. 6 - Label each double bond E, Z, or neither. (It may...Ch. 6 - Prob. 35CTQCh. 6 - Prob. 36CTQCh. 6 - Indicate the relationship between each pair....Ch. 6 - Prob. 38CTQCh. 6 - Prob. 1ECh. 6 - Prob. 2ECh. 6 - Using your model of butane (CH3CH2CH2CH3) ,...Ch. 6 - Consider the molecule 1-bromo-2-methylbutane. C3...Ch. 6 - Prob. 5ECh. 6 - Prob. 8ECh. 6 - Prob. 9ECh. 6 - Prob. 10ECh. 6 - Prob. 11ECh. 6 - Prob. 12ECh. 6 - Prob. 13ECh. 6 - Prob. 15ECh. 6 - Prob. 16ECh. 6 - Prob. 17ECh. 6 - Prob. 18ECh. 6 - Prob. 19ECh. 6 - Prob. 20ECh. 6 - Prob. 21ECh. 6 - Double bonds do not rotate freely under normal...Ch. 6 - up an example (not appearing in this ChemActivity)...Ch. 6 - Prob. 24ECh. 6 - Prob. 25E
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- 1. (6 points) Draw clear pictures showing the two chair conformations of this compound. Circle the lower energy (more stable) conformation or write "same energy". ||| |||arrow_forwardFor the 1,2-dichlorocyclohexane stereoisomers, which conformation of the trans stereoisomer has the lower energy, the diaxial or the diequatorial conformer? Which isomer and conformation of the three you built has the lowest energy? E of all the isomers of 1,2-dichlorocyclohexane. Explain the differences in energy, i.e., identify the sources of strain in the conformations you built. Show the sources of strain in a drawing.arrow_forwardSee attachment and solve the following a.) Draw the three staggered and three eclipsed conformations that result from rotation around the bond labeled in red using Newman projections.b.) Label the most stable and least stable conformation.arrow_forward
- Consider compound Q shown below (trimethylcyclohexane isomer). compound Q Which of the following is the most stable conformation of compound Q? I ||| CH3 Select one: O A. II OB. I O C. III O. D. IV H CH3 H CH3 H H- CH3 CH3 H CHS ||| H IV CH3 H CH₁ CH3 fff, H CH3 CH3 CH3arrow_forwardPlease answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. a.) Draw the most stable sawhorse conformation of cis-1,3-diphenylcyclohexane.b.) Draw the structure of meso-1,2-dimethylcyclopentane.arrow_forwardConsider compound Q shown below (trimethylcyclohexane isomer). compound Q Which of the following is the most stable conformation of compound Q? E ||| CH3 Select one: O A. II B. I O C. III D. IV H CH3 CH3 H H CH3 CH3 H CH3 || H CH3 CH3 H CH3 CH3 CH3 IV CH3 "f H Harrow_forward
- 5) relationship between the pairs of structures. NOTE: Each term may be used more than Choose the term from the five terms listed below that BEST describes the once and not all terms need be used. Identical Diastereomers Enantiomers Constitutional isomers Not isomers CH3 CH3 ÇI H3C-Br CH3 Br -CI H,C. D-H H3C- Br H- -D Br CH3 -CI ČH3 OH H3C, CHO OHC, OH OH H. HO CHO OHC CH3 H. OH ÓHarrow_forwardEthane spends all its time in the staggered conformation because it has the lowest potential energy. a. True b. False c. Neitherarrow_forward(7) In the box to the right of each structure, draw the lowest energy chair conformer. Work it out first on scrap paper. Please draw it with the t-Bu group pointing to the right...i.e. viewing each structure from the "bottom side of the ring".arrow_forward
- 4) Draw an alkene (minimum of 4 carbons) that is in the E conformation and a different alkene (also 4 carbon minimum) that is in the Z conformation. Provide an explanation as to what makes it E or Z.arrow_forwardPlease answer fast I give you upvote.arrow_forward1. Compound 1 is one isomer of 1,3-dicholoro-2,4,6-triisopropylcyclohexane. a) Draw both chair conformations of compound 1. State which is more stable. (An isopropyl group should be treated as 'larger' than a chloro group.) b) Draw the most stable achiral stereoisomer of this compound, in its most stable conformation. c) Draw the most stable chiral stereoisomer of this compound, in its most stable conformation. i-Pr i-Pr 1 i-Pr 'CIarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning