Help me with my study guide 6. Draw a molecule with each of the following characteristics: 1) a chiral carbon with (R) configuration; 2)a chiral carbon with an (S) configuration; 3) a tertiary amine; 4) a group that has torsional strain; 5) anester

Explanation:Chiral Carbon with (R) Configuration: The carbon atom bonded to the oxygen of the ester…

Answered: 6. Draw a molecule with each of the…

Chemistry & Chemical Reactivity

9th Edition

ISBN:9781133949640

Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel

Publisher:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel

Chapter23: Carbon: Not Just Another Element

Section23.3: Alcohols, Ethers, And Amines

Problem 2RC

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2. Using the following structures (all C7H120) as a guide, choose the ONE best answer for each of the following: OH OH C E F
For the following, you must draw an appropriate structure that has the chemical formula C5H,NO with the indicated functional group(s) and/or property. In each case, identify any other functional groups in the molecule you draw, that were not indicated in the question. You may use condensed dash or bond-line structure to draw your molecules. a) An aldehyde b) A cyclic ether c) An acyclic amide that cannot form hydrogen bonds with itself
REDRAW PROPOXYPHENE and LABEL the following: a) circle and label ALL functional groups presence in the molecule b) PROPOXYPHENE is optically active. Mark on the structure ALL the chiral centre(s) using (*) c) State the electronegative atom(s) that is/are able to form hydrogen bonds with water molecules d) Show ALL LONE PAIR(S) using symbol (LP) in PROPOXYPHENE molecule e) Determine the type of hybridization and the geometrical shape for carbon Y and Z that shows in the picture given.
Help me with my study guide
Example: Consider the naturally occurring amino acid, alanine, and its enantiomer.
A mixture contains equal amounts of compounds A–D. (See attachment) Question Which compounds alone are optically active?
5) Draw a different constitutional isomer of heptane (C₂H₁6) that contains a quaternary (4°) carbon. Then draw at least 3 other constitutional isomers.
Determine (A.) functional groups presents in the molecules and (B) determine the number of chiral carbons in the molecule (Exclude alkane) NH2 HO (Hint: Only six functional groups available)
18. Consider the following two compounds: CH3CH2CH2CH2CH3 and (CH3)2CHCH2CH3 Which statement below is INCORRECT? A) CH3CH₂CH₂CH₂CH3 has the higher boiling point. B) Greater surface area leads to more intermolecular attraction which results in a higher boiling point. C) (CH3)2CHCH2CH3 has the higher boiling point D) As the degree of branching increases, the surface area of the molecule decreases and the potential for intermolecular attraction via London forces decreases.
Q2. Write the number of chiral carbon atoms and the stereoisomers for the following compound. H3CH2C CH2CH3 Br H Br Number of chiral Carbon atoms Number of stereoisomers The structures of stereoisomers The relation between each two isomers if found
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6. Draw a molecule with each of the following characteristics: 1) a chiral carbon with (R) configuration; 2) a chiral carbon with an (S) configuration; 3) a tertiary amine; 4) a group that has torsional strain; 5) an ester