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1. (4 pts) On the line drawn below, provide the systematic (IUPAC) name for the following...
18. (15 pts) Nomenclature: Provide the systematic IUPAC name for each of the following molecules. Indicate...
18. (15 pts) Nomenclature: Provide the systematic IUPAC name for each of the following molecules. Indicate stereochemistry if applicable (Cis, Trans). 19. (6 pts) Draw all constitutional isomers of C&H Brz.
12. (5 pts) Nomenclature: Provide the systematic IUPAC name for each of the following molecules. Indicate...
12. (5 pts) Nomenclature: Provide the systematic IUPAC name for each of the following molecules. Indicate stereochemistry if applicable (R,S). CI
Write the IUPAC name for each of the compounds drawn below on the line provided. Be sure to include stereochemical infor...
Write the IUPAC name for each of the compounds drawn below on
the line provided. Be sure to include stereochemical information if
applicable (R, S, Cis, Trans, E, Z)
Instructions: write the IUPAC name for each of the compounds drawn below on the line provided. Be sure to include stereochemical information if applicable (R, S, cis, trans, E, Z) CI Cl Br
Instructions: write the IUPAC name for each of the compounds drawn below on the line provided. Be sure...
1) Provide the proper IUPAC name for the alkene shown below. CH2=CHCH2CH2CH2CH3 2) Provide the proper...
1) Provide the proper IUPAC name for the alkene shown below. CH2=CHCH2CH2CH2CH3 2) Provide the proper IUPAC name for the alkene shown below. 3) Draw an acceptable structure for 4-ethylhept-1-ene. 4) Provide an acceptable name for (CH3)2CHCH-C(CH3)CH2CH3. 5) Provide an acceptable name for (CH3CH2)2CHCH2CH-CH2. 6) Name the compound shown below. 7) Provide the proper IUPAC name for the alkene shown below. 8) Provide the proper IUPAC name for the alkene shown below. 9) Draw an acceptable structure for 4-phenylbut-l-ene. 10)...
17) Provide the proper IUPAC name for the alkene shown below 3-boro, A mutin agionavane 18)...
17) Provide the proper IUPAC name for the alkene shown below 3-boro, A mutin agionavane 18) Provide the proper IUPAC name for the alkene shown below CH" 19) Draw an acceptable structure for 4-phenylbut-1-ene. 20) Draw an acceptable structure for 1,2-dimethylcyclohexene. 21) Draw and name all alkenes which have the molecular formula C4Hs. 22) Name the alkene shown. Be sure to include the appropriate E or Z label necessary CH,CH 22) 23) 23) Provide a correct IUPAC name for the...
1. Provide a systematic IUPAC name for the compound, including R/S and E/Z if appropriate. (3...
1. Provide a systematic IUPAC name for the compound, including R/S and E/Z if appropriate. (3 pts.) 2. Draw the bond-line structure of (2,4Z)-2,5-dibromo-3-methylhexa-2,4-diene. (3 pts.) 3. Label the most stable and the least stable alkene (4 pts.) 4. Consider the substitution reaction below. (4 pts.) NaSH DMF SH in why this reaction proceeds through an SN mechanism and not an S2 mechanism a) Explain why this reaction proces o b) Explain why this reaction produces a racemic mixture of...
Question 1 4 pts Provide a systematic IUPAC name for this compound, including R/S and E/Z...
Question 1 4 pts Provide a systematic IUPAC name for this compound, including R/S and E/Z if appropriate. H Br (3E,5Z)-5-bromohepta-1,3,5-triene (35,5E)-5-bromohepta-1,3,5-triene (37,5E)-5-bromohepta-1,3,5-triene (32,5Z)-5-bromohepta-1,3,5-triene 4 pts Question 2
D Question 1 4 pts Provide a systematic IUPAC name for this compound, including R/S and...
D Question 1 4 pts Provide a systematic IUPAC name for this compound, including R/S and E/Z if appropriate. HH Br HYY HH (3E5Z)-5-bromohepta-1,3,5-triene (3E SE)-5-bromohepta-1,3,5-triene (37.5E)-5-bromohepta-1,3,5-triene (32.5Z)-5-bromohepta-1,3,5-triene
Provide the correct IUPAC/systematic name for the following compound.
Provide the correct IUPAC/systematic name for the following compound.
Provide the systematic (IUPAC) name for the following structure. OH my OH Show transcribed image text
Provide the systematic (IUPAC) name for the following structure. OH my OH
18. (15 pts) Nomenclature: Provide the systematic IUPAC name for each of the following molecules. Indicate stereochemistry if applicable (Cis, Trans). 19. (6 pts) Draw all constitutional isomers of C&H Brz.
12. (5 pts) Nomenclature: Provide the systematic IUPAC name for each of the following molecules. Indicate stereochemistry if applicable (R,S). CI
Write the IUPAC name for each of the compounds drawn below on
the line provided. Be sure to include stereochemical information if
applicable (R, S, Cis, Trans, E, Z)
Instructions: write the IUPAC name for each of the compounds drawn below on the line provided. Be sure to include stereochemical information if applicable (R, S, cis, trans, E, Z) CI Cl Br
Instructions: write the IUPAC name for each of the compounds drawn below on the line provided. Be sure...
1) Provide the proper IUPAC name for the alkene shown below. CH2=CHCH2CH2CH2CH3 2) Provide the proper IUPAC name for the alkene shown below. 3) Draw an acceptable structure for 4-ethylhept-1-ene. 4) Provide an acceptable name for (CH3)2CHCH-C(CH3)CH2CH3. 5) Provide an acceptable name for (CH3CH2)2CHCH2CH-CH2. 6) Name the compound shown below. 7) Provide the proper IUPAC name for the alkene shown below. 8) Provide the proper IUPAC name for the alkene shown below. 9) Draw an acceptable structure for 4-phenylbut-l-ene. 10)...
17) Provide the proper IUPAC name for the alkene shown below 3-boro, A mutin agionavane 18) Provide the proper IUPAC name for the alkene shown below CH" 19) Draw an acceptable structure for 4-phenylbut-1-ene. 20) Draw an acceptable structure for 1,2-dimethylcyclohexene. 21) Draw and name all alkenes which have the molecular formula C4Hs. 22) Name the alkene shown. Be sure to include the appropriate E or Z label necessary CH,CH 22) 23) 23) Provide a correct IUPAC name for the...
1. Provide a systematic IUPAC name for the compound, including R/S and E/Z if appropriate. (3 pts.) 2. Draw the bond-line structure of (2,4Z)-2,5-dibromo-3-methylhexa-2,4-diene. (3 pts.) 3. Label the most stable and the least stable alkene (4 pts.) 4. Consider the substitution reaction below. (4 pts.) NaSH DMF SH in why this reaction proceeds through an SN mechanism and not an S2 mechanism a) Explain why this reaction proces o b) Explain why this reaction produces a racemic mixture of...
Question 1 4 pts Provide a systematic IUPAC name for this compound, including R/S and E/Z if appropriate. H Br (3E,5Z)-5-bromohepta-1,3,5-triene (35,5E)-5-bromohepta-1,3,5-triene (37,5E)-5-bromohepta-1,3,5-triene (32,5Z)-5-bromohepta-1,3,5-triene 4 pts Question 2
D Question 1 4 pts Provide a systematic IUPAC name for this compound, including R/S and E/Z if appropriate. HH Br HYY HH (3E5Z)-5-bromohepta-1,3,5-triene (3E SE)-5-bromohepta-1,3,5-triene (37.5E)-5-bromohepta-1,3,5-triene (32.5Z)-5-bromohepta-1,3,5-triene
Provide the correct IUPAC/systematic name for the following compound.
Provide the systematic (IUPAC) name for the following structure. OH my OH
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