Organic ChemistryMaxwellpresented by Macmillan LearningClassify the pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric.Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each.H3CHCH3H3C.CI.CIH3CCompound 1Compound 2The compounds areO enantiomersO identicalO diastereomersO constitutional isomersO not isomericThe correct IUPAC names are:O Compound 1: (2S,3R)-2,3-dichlorobutane Compound 2: (2R,3S)-2,3-dichlorobutaneO Compound 1: (2R,3R)-2,3-dichlorobutane, Compound 2: (2R,3S)-2,3-dichlorobutaneO Compound 1: (2S,3S)-2,3-dichlorobutane, Compound 2: (2R,3R)-2,3-dichlorobutaneO Compound 1: (2R,3S)-2,3-dichlorobutane, Compound 2: (2S,3R)-2,3-dichlorobutane48°F Light raF5F6PrtScnHomeEndPgUpF7F8F9PgDcF10F11

According to the given data we need to determine the isomer and the IUPAC of those compounds

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Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter6: Alkanes & Alkenes

Section: Chapter Questions

Problem 4E: Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This...

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DZL Announcements - CHM240-201 ↑ Q X 82°F Partl app.101edu.co Organic Chemistry Draw all of the stereoisomers of 3-bromo-5-methylheptane. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Select to Draw an Isomer x Select to Draw an Isomer Aktiv Chemistry Q
Indicate whether the pair of structures shown represent stereoisomers, constitutional isomers, different conformations of the same compound, or the same conformation of a compound viewed from a different perspective. Note that cis, trans isomers are an example of stereoisomers. CH3 CH3 CI CI H H H. H CH3 H. H' H. CH3 Submit Answer Retry Entire Group 6 more group attempts remaining (Previous Next Save and Exit Cengage Learning | Cengage Technical Support MacBook Air DII 888 F12 F10 F7 F4 & 9 delete - 4 5 6 8 { т Y U P F G J K 1r command eption .. ..
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Explain the properties of Constitutional isomers ?
5) Use compounds X, Y and Z (shown below) to answer the following questions. H. H3C" "CH3 ОН CH3 compound X compound Y compound Z a) Is compound X classified as cis, trans or neither? b) Is compound Y classified as E, Z or neither? c) Is compound Z classified as R, S or neither? d) Are compounds X and Y constitutional isomers of each other? (YES or NO) e) Are compounds Y and Z constitutional isomers of each other? (YES or NO) f) Classify compound Y as a primary, secondary or tertiary alcohol. g) Which compound(s) is(are) chiral? h) Give the IUPAC name for compound Z, omitting the absolute configuration (R or S) designation. i) In the indicated spaces below, draw stereoisomers of compounds X, Y and Z. stereoisomer of compound X stereoisomer of compound Y stereoisomer of compound Z
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Classify each attached pair of compounds as constitutional isomers or identical molecules.
Which of the following line drawings represents the correct stereochemistry o molecule shown in the Newman projection below? E + Н. H I CH₂CH3 LOH H CH3 OH OH || IV OH 5.... OH A) I B) II C) III D) IV K
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O Macmillan Learning Indicate whether each pair of structures represents the same compound, structural isomers (also called constitutional isomers), or different compounds. and Zoth and
How many isomers (structural, geometric, and tereo) have the formula C5H10, and have "cyclo" in their name? (i.e. they contain a ring) 06 0 5 07 04 03
None of the above 5 Which of the following statements are comect? 1-Stability of conformation is affected due to torsional strain. Il-Magnitude of torsional strain depends upon, the angle of rotation about C-Cbond. III-In case of solid alkenes the Trans andCsisomershave different physical properties IV In case of solid alkenes the Trans and Cs isomers have the same physical properties I and II Al Pue 1. Il and III 孔曲and V None of the above

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