Circle the "isoprene" units in the following terpene. Label the head (h) and tail (1) of each "isoprene" unit. Finally, state the compound's terpene classification. CH3 H,C H,C CH3 classification:
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- Write the IUPAC name of the following molecule: *Lowercase letters only and DO NOT put space in between. Gray balls represent C, white balls represent H, green ball represent F. Do not include stereochemistry.Please draw the line structures for the C8H17+ carbocations that have the carbon skeleton below And please circle the most stable carbocationFor Tylenol (Acetaminophen), what is the primary and secondary carbon? Any enantiomers? (R and S)
- In 1935, J. Bredt, a German chemist, proposed that a bicycloalkene could not have a double bond at a bridgehead carbon unless one of the rings containsat least eight carbons. This is known as Bredt’s rule. Explain why there cannot be a double bond at this position.Consider the molecule: rate the priority functional groups from highest to lowest A. Alkyl chain B. Ketone C. Carbonyl D. AnhydrideIn 1935, J. Bredt, a German chemist, proposed that a bicycloalkene could not have a double bond at a bridgehead carbon unless one of the rings contains at least eight carbons. This is known as Bredt’s rule. Explain why there cannot be a double bond at this position.
- How many lone pairs are involved in sustaining the conjugation of pyridine?Will the cyclopropane formed be facing same direction as substituents or away?(will it have dashed wedges)?Which boiling point and melting point is the higher between cis-1,3-dimethylcyclobutane and trans-1,3-dimethylcyclobutane? Explain.
- Give IUPAC name of the following molecule and indicate Z or E. Answer all four of themClassify attached carbocation as 1°, 2°, or 3°.Write the IUPAC name of the following molecule: *Lowercase letters only and DO NOT put space in between. Gray balls represent C, white balls represent H. Do not include stereochemistry.