Task 7 - Draw the two enantiomers of following:3-methyl hexane1. Locate the chiral centre2. Draw one3. Draw its mirror image beside it.enantiomer in atetrahedral shapeHHCH3 HHC.C-H.H.H.H.H.H.H1-chloro-3-methyl pentane2. Draw one3. Draw its mirror image beside it.enantiomer in atetrahedral shape1. Locate the chiral centreCIHCH3 HH FC-C.C-HHHH.H2. Draw one enantiomerin a tetrahedral shape3. Draw its mirror image beside it.2-chlorobutane1. Locate the chiral centreH.CIH.H-C ▬C-HH.H Drawing optical isomers1. Locate the chiral centre- look for the carbon atom with four different groupsattached.2. Draw one enantiomer in a tetrahedral shape-chlo1. Loca- put the chiral carbon atom at thecentre and the four different groups in a tetrahedral shape around it. Don't try to drawthe full structure of each group -it gets confusing, Just use the structural formulas.3. Draw the mirror image of the enantiomer-put in a mirror line next to theenantiomer and then draw the mirror image of the enantiomer on the other side of it.ExampleDraw the two enantiomers of 2-hydroxybutanoic acid. The structure of 2-butanoic acid isshown below.1. Locate the chiral centre2. Draw one3. Draw its mirror image beside it.enantiomer in a1. Latetrahedral shapeHHHC.CH,CHICOOHC*COOHchiral centreHH.OHH;CH,CI HOOCH;CH,CОНOHОН

Answered: Image /qna-images/answer/c56b2945-3c46-4c43-9b5f-eb45139c726b.jpg

Task 7- Draw the two enantiomers of following: 3-methyl hexane 1. Locate the chiral centre 2. Draw one 3. Draw its mirror image beside it. enantiomer in a tetrahedral shape H. CH3 H H. H. C FC -C C. C C- H H H H H H. H. 1-chloro-3-methyl pentane 3. Draw its mirror image beside it. 2. Draw one 1. Locate the chiral centre enantiomer in a tetrahedral shape Cl CH3 H H -C C- H H 2. Draw one enantiomer 3. Draw its mirror image beside it. 2-chlorobutane in a tetrahedral shape 1. Locate the chiral centre H CI H. H -C C C- H- H. H. H

Task 7- Draw the two enantiomers of following: 3-methyl hexane 1. Locate the chiral centre 2. Draw one 3. Draw its mirror image beside it. enantiomer in a tetrahedral shape H. CH3 H H. H. C FC -C C. C C- H H H H H H. H. 1-chloro-3-methyl pentane 3. Draw its mirror image beside it. 2. Draw one 1. Locate the chiral centre enantiomer in a tetrahedral shape Cl CH3 H H -C C- H H 2. Draw one enantiomer 3. Draw its mirror image beside it. 2-chlorobutane in a tetrahedral shape 1. Locate the chiral centre H CI H. H -C C C- H- H. H. H

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

1. How are the following compounds related (Identical, enantiomers, diastereomers, constitutional isomers, unrelated) COOH a. CI Br Br b. C, CI .....||COOH H Br H Br COOH Br COOH NH2 NH2 H- -OH HO -H H- -OH H -OH CH3 d. CH3 Br
For the molecule below: 1. Identify all CHIRAL centers if any are present: 2. Name each CHIRAL center (R or S if they exist): bottom O O top O A B E L A: NO chiral centers B: One chiral center: R C: One chiral center: S D: Two chiral centers: (top) R and (bottom) S E: Two chiral centers: both RR F: Two chiral centers: (top) S and (bottom) R G: Two chiral centers: both SS
III. Consider the compound below. CH, CI- Br но O- H. (Atomic number: H-1, C-6, O-8, CI-17, Br-35) a. How many chiral centers are in the molecule? b. How many stereoisomers are there for the compound? c. Draw the Fischer projection for each of the stereoisomer and determine the absolute configuration (R or S). Label each using I, II, etc. d. Which pairs are enantiomers? Which are diastereomers?
36-39. Identify the type of stereoisomerism Choices: A. conformational diastereomers B. enantiomers C. constitutional isomers D. configurational 36. 37. 39. H3C 38. H3CH₂C Br CH3 H H3C Br H CH3 H CH₂CH3 CH3 diastereomers CI CH3 H3C H3C H₂ I Br Br CH3 CH3 Br CH3 CH3 CH₂CH3
Using the isomers below: H OH HO H HO3 HO H a. Identify the chiral centers and label the absolute configuration of each chiral carbon atom below as R or S. b. Draw each isomer above as Newman projections from the C3-C4 perspective. c. Draw each isomer as a Sawhorse projection from the C3-C4 perspective
Q6. Encircle the structures of all the chiral molecules drawn below and assign absolute configuration (R/S) to all the chiral atoms. Draw the Fischer projections of the enantiomers of all these molecules except epoxides. OH OH OH CH, H,C CH, CH, H,C H,C OH OH OH CH, H,C CH, CH
3.) For each of the following structures, star any chiral centers and label each chiral center as (R) or (S). b. H CH3 a. с. CH, ço,H HO. H3C Br CH2SH H H NH2 OH
2. What term best describes how the following structures/molecules are related to each other? Enantiomers Br b. Diastereomers c. Identical d. Constitutional Isomers سال Br Br Br
Which of the following statements is/are correct? Br Br Br Br CI 'P' 'R' 'S' .D. A. P and Q are non-superimposable mirror images of each other. B. R and S are non-superimposable images of each other. C. Q and R are same compound. D. Q and S are enantiomers. E. statements A and B are correct.
1. a.) Put asterisk on chiral centers b.) Label each chiral center as R or S. c.) Draw the enantiomer d.) Draw one diastereomers H N. N- H N. ÕH CONH, O NH (CH3)3C
5. Determine whether each of the compounds shown below is chiral or achiral and optically active or inactive. Finally, determine the absolute configuration of any chirality centers. a. b. HS C. H SH Cl a. chiral or achiral? a. opt. active or inactive? b. chiral or achiral? b. opt. active or inactive? H H₂N CH3 H CH₂CH3 c. chiral or achiral? c. opt. active or inactive?
1. For the structure below, assign the chiral centers with R/S configurations. Draw an enantiomer and diastereomer. Convert the original structure to Fischer Projection. OH HO NH₂