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5. Using your models, verify whether the following two compounds are the same compound or constitutional...
Give the relationship of the two compounds: Different Compounds, Same compound, Constitutional (structural) isomers, Enantiomers, or...
Give the relationship of the
two compounds: Different Compounds, Same compound, Constitutional
(structural) isomers, Enantiomers, or Diastereomers
d) (4 pts) CH3 CH(CH3)2 H-CH2CH3 BrH Br H+CH2CH2 CH(CH3)2 CH3 e) (4 pts)
Name: Doom! CH3 Part 2: Isomers - Pairs of compounds. Structural Isomers: 1. Use your model...
Name: Doom! CH3 Part 2: Isomers - Pairs of compounds. Structural Isomers: 1. Use your model kit and build both of these structure. CH3 CH3-CH2-CH2 CH3-CH-CHE A. B. 1 What is the molecular formula for compound A? What is the molecular formula for compound B? - Without breaking any bonds, is it possible to convert A into B? Would the two compounds have identical properties?! What is the IUPAC name for compound A? What is the IUPAC name for compound...
Give the relationships between the following pairs of structures. State whether they represent the same compound,...
Give the relationships between the following pairs of
structures. State whether they represent the same compound,
different compounds, or they are constitutional isomers of each
other.
Give the relationships between the following pairs of structures. State whether they represent the same compound, different compounds, or they are constitutional mers of each other CH2C1CHCICH3 and CH CHCic H2C1 (ii) and Gii) CH2- CHCH2CH and iv CH3CH2CHClCH2C1 and CH3CHCH2Cl HeCl
Classify the following pair of compounds as the same compound, enantiomers, diasteromers, constitutional isomers, or not...
Classify the following pair of compounds as the same compound, enantiomers, diasteromers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each. same compound enantiomers diastereomers constitutional isomers not isomeric The correct IUPAC names are: Compound I: (3S, 4S)-3,4-dimethylheptane, Compound II: (3S, 4S)-3,4-dimethylheptane Compound I: (3R, 4S)-3,4-dimethylheptane, Compound II: (3S, 4S)-3,4-dimethylheptane Compound I: (3R, 4S)-3,4-dimethylheptane, Compound II: (3S, 4S)-3,4-dimethylheptane Compound I (3S, 4S)-3,-4-dimethylheptane, Compound II: (3R, 4S)-3,4dimethy/heplane
Classify the following pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not...
Classify the following 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. same compound enantiomers diastereomers constitutional isomers not isomeric The correct IUPAC names are: Compound 1: (3R.4S)-3,4-dimethylheptane, Compound II: (3S,4R)-3,4-dimethylheptane Compound I: (3S,4S)-3,4-dimethylheptane, Compound II: (3S,4S)-3,4-dimethylheptane Compound I: (3R.4S)-3,4-dimethylheptane, Compound II: (3S,4S)-3,4-dimethylheptane Compound 1: (3S,4S)-3,4-dimethylheptane, Compound II: (3R.4S)-3,4-dimethylheptane
a. For each pair of compounds, tell whether the structural formulas shown represent the same compound,...
a. For each pair of compounds, tell whether the structural formulas shown represent the same compound, different compounds that are constitutional isomers or different compounds that are not constitutional isomers. [4 x 1 mark] (1) and (11) and (111) and (iv) and b. Draw a structural formula for each compound. 1 (3E, 62) 2,9-dimethyl-3,6-decadiene (i) 1,6-Heptadiyne (111) 3-phenyl-1.3-butanediol [1 mark] [1 mark] [1 mark] c. Give TWO chemical tests which are indicated by a change in colour, (write the equation...
Classify the following pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not...
Classify the following 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. same compound enantiomers diastereomers constitutional isomers not isomeric The correct IUPAC names are: Compound I: (2S, 3S)-1, 2, 3-tribromobutane, Compound II: (2R, 3S)-1, 2, 3-tribromobutane Compound I: (2R, 3S)-1, 2, 3-tribromobutane, Compound II: (2S, 3S)-1, 2, 3-tribromobutane Compound I: (2R.3RH, 2, 3-tribromobutane, Compound II: (2S, 3R)-1, 2, 3-tribromobutane...
please explain your answers 11. Indicate whether the pairs of compoun whether the pairs of compounds...
please explain your answers
11. Indicate whether the pairs of compoun whether the pairs of compounds shown below are enantiomers, diastereomers, structural (constit. ructural constitutional) isomers, the same compound, or different compounds which are not isomers. (0.25 pts ea = 1 pt) Structural H OH Vs. constitutional но н OH CHE H OH vs. dia stereomers BE BroH. H₂CH₂CH CH3 HOCH2 CHO here the we dia stereomers distoremos он он носна сно н CNHO VS HOC 2 TNH₂ CH SH...
Week 10- Constitutional isomers Constitutional isomers have the same molecular formula, but their atoms are bonded...
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...
onsider each pair of molecules below. State whether they represent the same compound (identical), whether they...
onsider each pair of molecules below. State whether they represent the same compound (identical), whether they are different molecules with the same molecular formula (constitutional isomers), or whether they are different molecules that are not isomeric (different molecular formulas- neither). (2 pts each) H2CCH2 H2CCH2 CH3 b) он H2 FCH CH CH2F H3C erther conshtuhonal isomers /22
Give the relationship of the
two compounds: Different Compounds, Same compound, Constitutional
(structural) isomers, Enantiomers, or Diastereomers
d) (4 pts) CH3 CH(CH3)2 H-CH2CH3 BrH Br H+CH2CH2 CH(CH3)2 CH3 e) (4 pts)
Name: Doom! CH3 Part 2: Isomers - Pairs of compounds. Structural Isomers: 1. Use your model kit and build both of these structure. CH3 CH3-CH2-CH2 CH3-CH-CHE A. B. 1 What is the molecular formula for compound A? What is the molecular formula for compound B? - Without breaking any bonds, is it possible to convert A into B? Would the two compounds have identical properties?! What is the IUPAC name for compound A? What is the IUPAC name for compound...
Give the relationships between the following pairs of
structures. State whether they represent the same compound,
different compounds, or they are constitutional isomers of each
other.
Give the relationships between the following pairs of structures. State whether they represent the same compound, different compounds, or they are constitutional mers of each other CH2C1CHCICH3 and CH CHCic H2C1 (ii) and Gii) CH2- CHCH2CH and iv CH3CH2CHClCH2C1 and CH3CHCH2Cl HeCl
Classify the following pair of compounds as the same compound, enantiomers, diasteromers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each. same compound enantiomers diastereomers constitutional isomers not isomeric The correct IUPAC names are: Compound I: (3S, 4S)-3,4-dimethylheptane, Compound II: (3S, 4S)-3,4-dimethylheptane Compound I: (3R, 4S)-3,4-dimethylheptane, Compound II: (3S, 4S)-3,4-dimethylheptane Compound I: (3R, 4S)-3,4-dimethylheptane, Compound II: (3S, 4S)-3,4-dimethylheptane Compound I (3S, 4S)-3,-4-dimethylheptane, Compound II: (3R, 4S)-3,4dimethy/heplane
Classify the following 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. same compound enantiomers diastereomers constitutional isomers not isomeric The correct IUPAC names are: Compound 1: (3R.4S)-3,4-dimethylheptane, Compound II: (3S,4R)-3,4-dimethylheptane Compound I: (3S,4S)-3,4-dimethylheptane, Compound II: (3S,4S)-3,4-dimethylheptane Compound I: (3R.4S)-3,4-dimethylheptane, Compound II: (3S,4S)-3,4-dimethylheptane Compound 1: (3S,4S)-3,4-dimethylheptane, Compound II: (3R.4S)-3,4-dimethylheptane
a. For each pair of compounds, tell whether the structural formulas shown represent the same compound, different compounds that are constitutional isomers or different compounds that are not constitutional isomers. [4 x 1 mark] (1) and (11) and (111) and (iv) and b. Draw a structural formula for each compound. 1 (3E, 62) 2,9-dimethyl-3,6-decadiene (i) 1,6-Heptadiyne (111) 3-phenyl-1.3-butanediol [1 mark] [1 mark] [1 mark] c. Give TWO chemical tests which are indicated by a change in colour, (write the equation...
Classify the following 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. same compound enantiomers diastereomers constitutional isomers not isomeric The correct IUPAC names are: Compound I: (2S, 3S)-1, 2, 3-tribromobutane, Compound II: (2R, 3S)-1, 2, 3-tribromobutane Compound I: (2R, 3S)-1, 2, 3-tribromobutane, Compound II: (2S, 3S)-1, 2, 3-tribromobutane Compound I: (2R.3RH, 2, 3-tribromobutane, Compound II: (2S, 3R)-1, 2, 3-tribromobutane...
please explain your answers
11. Indicate whether the pairs of compoun whether the pairs of compounds shown below are enantiomers, diastereomers, structural (constit. ructural constitutional) isomers, the same compound, or different compounds which are not isomers. (0.25 pts ea = 1 pt) Structural H OH Vs. constitutional но н OH CHE H OH vs. dia stereomers BE BroH. H₂CH₂CH CH3 HOCH2 CHO here the we dia stereomers distoremos он он носна сно н CNHO VS HOC 2 TNH₂ CH SH...
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...
onsider each pair of molecules below. State whether they represent the same compound (identical), whether they are different molecules with the same molecular formula (constitutional isomers), or whether they are different molecules that are not isomeric (different molecular formulas- neither). (2 pts each) H2CCH2 H2CCH2 CH3 b) он H2 FCH CH CH2F H3C erther conshtuhonal isomers /22
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