Answer) constitutional isomers
Explanation:
The first molecule is numbered from left to right. It is the longest chain. the longest carbon chain contains 10 carbon atoms therefore the parent chain name is Decane . There are one ethyl substituent at 8 carbon, two methyl substituent at 3rd and 6th carbon and one propyl substituent at 4th carbon atom. Therefore, the IUPAC name is 8-Ethyl-3,6-dimethyl-4-propyldecane.
The second molecule is numbered from bottom to up. It is the longest chain. The longest carbon chain contains 11 carbon atoms. Therefore, the parent chain name is undecane. There are two methyl substituent at 2nd and 5th carbon atom and two ethyl substituent at third and seventh carbon atom , therefore the IUPAC name is 3,7-diethyl-2,5-dimethylundecane.
Both the molecules have different names because of the different connectivity of atoms therefore these molecules are constitutional (structural) isomers. Structural isomers have same molecular formula and different structural formula. Bothe these molecules have molecular formula C17H36 But their structures are different.
Therefore they are not the same molecule.
3. Determine whether the following pair of molecules are representations of the same molecule, or if...
please help with both questions
Clearly assign priorities ( 1-4) for the substituents attached to the mark following molecules. (You do NOT need to determine R or S. Just assign priorities.) ed chirality center in each of the 1. он NH2 2. Circle (or ighlight) all chirality centers in a derivative of progesterone, a cortisone like molecule (shown). Make sure locate all the H's on the molecule first. но- он OH
Clearly assign priorities ( 1-4) for the substituents attached...
identifying and designating chirality
Clearly assign priorities (1-4) for the substituents attached to the marked chirality center in each of the following molecules. (You do NOT need to determine R or S. Just assign priorities.) 1. Он Circle (or highlight) all chirality centers in progesterone, an estrogen like molecule (shown) 2. Make sure locate all the H's on the molecule first. Page 1 of 2 пн
Please refer to the following structure to answer questions 5-7 CH3 ci Cis 5. What is the relationship of the substituents to one another b. Trans c. No Relationship 6. True or False: There are no 1,3-diaxial interactions in the current structure 7. True or False: The other conformation as a result of the ring flip will not have any 1,3-diaxial interactions 8. For each pair of structures shown indicate whether the two structures are constitutional isomers, enantiomers, diastereomers, or...
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 CH3 Ć Ći Click on all of the carbon chirality centers in the molecule below. (Other terms used for chirality center include chiral center, stereocenter, and stereogenic center.) If no carbon qualifies, submit your answer without selecting any. H3C...
Problem 10 Consider the following pair of structures. Designate each chirality center as (R) or (S) and identify the relationship between them by describing them as representing enantiomers, diastereomers, constitutional isomers, or two molecules of the same compound. CH,CHз CH-CHз pue CH3CH2 CH3CH2
4. For each pair of molecules, assian the confiquration at each chiral center as R or S Give the relationship between the pair of molecules es no relation, constitutional isomers, same molecule but not meso, some molecule and meso, enantiomers, or diastereomerS There should only be one possible answer. OH OH Constitutiona Soenars b. Br Br c. NH2 NH2 NH2 NH2 d. HO. но. ШЕи ши.
Indicate whether each of the following molecules R, S, Z or E. Label the substituents according to priority. The third molecule is a Fischer projection. Cl H2C SH H CH3 CH3 Label each pair of molecules as enantiomers, diasteromers, identical molecules constitutional isomers, or not isomers at all. No partial credit. H3C SH CH3 CH(CH3)2 H3C CH2CH2F CH(CH3)2 H3C CH2CH3 and H CH3 and H SH Cl HOH OH and CH3
Examine the following molecules, and circle any that are chiral. Then, draw a box around any meso compounds. 4. CH3 он H2N H3 Br CH он CI он H O NH 5. Assign the absolute configuration (Ror S) to each stereogenic center in the following chiral molecules using the Cahn-Ingold-Prelog priority rules
I have completed some answers! I just really really need help
with the rest! I am so lost! please help me, if you can!
What information do you need? Can you see the pictures that I
posted?
#2-6 are using the FIGURE from question #2
#7-8 go together and uses #7 FIGURE
#9-12 uses #9"s FIGURE but #11 and #12 compares the two FIGURES
from #7	
#13 and 14 are together
# 15 and # 16 are their own problems...
Question 3 (1 point) What is the relationship between the following molecules? Br Br Same compound. Pair of enantiomers. Pair of diastereomers. Unrelated. Two of the above. Question 4 (1 point) Saved Which of the following molecules has stereogenic center with configurati Br estion 4 (1 point) ✓ Saved Which of the following molecules has stereogenic center with configuration R? Br o Br Question 5 (1 point) Which of the following is true regarding 50/50 mixture of the following molecules?...