A) Identical.
Since both the functional groups ( -NH2 and -CH2OH) are above the plane in both structures and position of double bond is same.
The OH is attached to achiral center, so its position does not matter.
B) Diastereomers but not epimers
Cis-trans isomers have different configuration and are not mirror images to each other.
Epimers differ in their configuration at chiral centre. Since there is no chiral center in cis-trans or E/Z isomer, this is not an epimer.
C) Enantiomer
Stack the two molecules on each other and place a mirror in between them. All the -OH groups will be reflected. So, the given compounds are mirror images of each other and does not super-impose on each other.
D) Enantiomer
Keep the molecules as it is (sideways) and place a mirror in between the two molecules. The molecules are mirror images and does not super-impose on each other.
E) Constitutional isomers
Constitutional isomers have different atom to atom connectivity. This includes positional, structural and functional isomers.
The given compounds differ in functional groups. First has aldehyde group while second has ketone group.
Part C: Identify the chirall centers and relationship between each part of Your choices are not...
Describe the relationship between the following two molecules: Он H H он но н Он Diastereomers Conformational isomers Enantiomers Constitutional isomers Identical molecules Tries 0/1 Submit Answer Describe the relationship between the following two molecules: Enantiomers A meso compound Diastereomers Identical molecules Constitutional isomers Conformational isomers Tries 0/1 Submit Answer
3. Identify the relationship between each of the following pairs of molecules as constitutional isomers, enantiomers, diastereomers, or meso compounds. CH3 но - оноо но Х он но -н. H2NH H- H CH3 осон BiH HO н+он н-он ну он Br +н CH3 CH3 HOTH HO HỌ NH2 NH, HẠNH I но НЕН CH3 I H- H нон н +он но -н CH3 HO на
Question 9 15 pts Determine the relationship between each set of structures Set 1: identical Set 2: constitutional isomers Set 3: diastereomers Set 4: diastereomers Set 5: enantiomers 2 OH OH OH e HO... г - 2 ОН ОН ОН Но... 3 ОН Н. СІ НО, CI нс H нс ОН ОН H 5 н- H CHO -ОН ОН CH2OH CHO но- -Н Н- -ОН Сн,ОН Е.
3. Identify the relationship between the pairs of molecules shown below as either: the same molecule, diastereomers, enantiomers, or epimers. (3 points each) CH2OH СНОн он но -н H-OH он OH он OH OH OH H2OH CH2OH 4. Draw the Line Angle formula for the products of the following reactions. (4 points each) Cu+2 -Cu2O(s) + + но -н CH2OH Ht, heat OH HO heat
Describe the relationship between the following two molecules: ОН O Identical molecules O Conformational isomers o Constitutional isomers O A meso compound O Enantiomers O Diastereomers Submit Answer Tries 0/1 Describe the relationship between the following two molecules: но OH O Identical molecules O Enantiomers Constitutional isomers O Conformational isomers O Diastereomers O A meso compound Submit Answer Tries 0/1 Describe the relationship between the following two molecules: SH O Conformational isomers O Diastereomers Enantiomers O Constitutional isomers O A...
The relationship between I and II is: ________. diastereomers enantiomers same compound constitutional isomers CH2OH CH2OH но н н он нон HOHн CH2OH CH2OH ОН
Question 35 (2.5 points) What is the relationship between the following compounds? н он н он но н но ༢ ཙ ༩ ། O diastereomers enantiomers identical compounds constitutional isomers O completely unrelated compounds Question 36 (2.5 points) Consider the following molecule with its shown stereochemistry. What positions do the substituents occupy when the molecule in its most stable conformation? 1: axial 2: equatorial O 1:equatorial 2: axial 1: axial 2: axial all of the above are equally stable. 1:equatorial...
What is the relationship between each pair of molecules shown below? H Н3САН нсH3 CH3 identical constitutional isomers enantiomers diastereomers no relationship OH CH3 HO|| І. ОН CH3 CH3 НО! исHз с. тісі
Relationship for each picture: Identical, constitutional isomers, enantiomers, diasteromers, or not related (not isomers) с CHO он CHOCI он CHCI ОН Н. НО H CHO он H -CH, CH, сон НО сн. сон
Identify the relationship between the structures shown [1] Same compound drawn differently ш HO Constitutional isomers Enantiomers НО Diastereomers [2] Same compound drawn differently Constitutional isomers Enantiomers Diastereomers [3] Same compound drawn differently Constitutional isomers Enantiomers Diastereomers [4] Same compound drawn differently Br Constitutional isomers Br Enantiomers Diastereomers