Give the relationship between each pair of molecules of the formula C5H6ClF. Your options are constitutional...
5. Identify the type of isomeric relationship between each pair of molecules below, from the following five choices (arranged from least to most similar): not isomers, constitutional isomers, geometric isomers, conformers, identical. CH3 CH2 CH3 HH CH D CH₂ Η γH HTYCH, CH DDO NOT ANSWER THIS ONE н H₃G. CH₂CH₂ н сн, CC and C= C HH CH3CH2 H - 125 - CA31
Name the isomeric relationship (enantiomers, constitutional isomers, identical, or diastereomers) for each pair of molecules. and &-á e dua and 3. C! and OH Br- H Br H and ОН H- Br H+Br CH3 CH3
Choose the best term that best describes the relationship between this pair of molecules a) enantiomers b) diastereomers c) conformers d) constitutional isomers e) identical 2) Choose the best term that best describes the relationship between this pair of molecules (1 mark) CH; Hz H H C-¢---Br Br--C-¢-C - H Å a) enantiomers b) diastereomers c) conformers d) constitutional isomers e) identical
9. Classify each pair of compounds as identical molecules stereoisomers, constitutional isomers or not isomers of each other. and OH H and C₂Hs Ćato and 22 10. Which of the following compounds are meso? Explain ' & BrCI OH (A) (B) (C) (D)
1. Identify each pair of compounds as constitutional isomers, stereoisomers, identical molecules, or other. (a) stereoisomers constitutional isomers other identical molecules (b)identical molecules other stereoisomers constitutional isomers (c) constitutional isomers identical molecules stereoisomers other (d)other identical molecules constitutional isomers stereoisomers
Week 10- Constitutional isomers Constitutional isomers have the same molecular formula, but their atoms are bonded in different orders. These may be further distinguished as chain isomers, which differ only in hydrocarbon chain structure, positional isomers, which differ in the location of a functional group, and functional group isomers which differ in the nature of their functional groups. Typically chain and position isomers show only modest differences in their physical and chemical properties, while functional group isomers differ greatly from...
Classify each pair of compounds as constitutional isomers, stereoisomers, or identical molecules. H3C-CH2 CH3 H3C-CH2 Classify: and O constitutional isomers Ostereoisomers O identical molecules CH3 H3C Classify: H2C-CH2-CH-CH-CH3 and н, с CH-CH-CH, CH3 ан. CH3 CH3 O constitutional isomers stereoisomers identical molecules Classify: H₂C. and сн. НАС O identical molecules stereoisomers O constitutional isomers
A. (b) Identify structure(s) for all constitutional isomers with the molecular formula C4Hg that have one double bond. Select all that apply. H H H C. H C - 0- 0- 0- H H-CC=C—CH H H H H. H H H H -6-I || IT Itt I H H I- B. H C - C= C- H H- C= C— C— C— H - 0-II II HHHH HC-H Which of the following is a constitutional isomer of cyclopropane? н. Н...
For each pair of isomers in the table below, indicate the type of isomerism that is present from the following list: chain, position, functional group, geometric (cis-trans), enantiomer 2. OH CH3CH2CH2OH CHяCHCHз CH3CH2OH CH30CH3 COOH HOOC Нас н он Hu C CHз но CI H H H CH3 CH3CH2CH2CH3 CH3CHCH3 3. Write the systematic IUPAC name of the compound:
I 17 points shown below is the lipid lowering drue simvastatin, which contains soven chical centers stereogeni centers incle all the stereocenter Points will be deducted for incorrecta mente HO ICH HC Simvastatin (Lipid-lowering agent) 2.14 points) Give the complete IUPAC names, including Ror Sconfiguration for the following molecules IUPAC name (include Ror S) IUPAC name (include Ror S) 3. (4 points) Using dashed wedge representations, give the structures of the following molecules (5)-2-Bromopentane (R)-2-Pentanol Questions 4 & 5 relate...