Consider that cyclobutane exhibits a puckered geometry. Judge the relative stabilities of the 1,2-disubstituted cyclobutanes and of the 1,3-disubstituted cyclobutanes.

DRAW THE COMPOUNDS WITH THE FOLLOWING IUPAC NAMES...

Why do 1-methylcyclohexene and 3-methylcyclohexene have a lower boiling point than 2-methylcyclohexanol?

Organic Chemistry Incorrect Separation Scheme Cannot be hand-drawn  *see attached for the incorrect separation scheme provided. The top of the separation scheme shows what other compound is mixed with your molecule (2,6-dimethyloct-2-ene). Assume for the purposes of this assignment that both compounds are solid at room temperature. Also assume that both compounds are soluble in ether, except ionic compounds.  The goal of the separation is the isolate each of the two compounds from the mixture. Below the incorrect separation scheme write a discussion of this incorrect scheme identifying all of the mistakes in the separation scheme. Keep in mind that there will be more than one mistake in the scheme. For each mistake, give a detailed, scientific explanation of why it is incorrect.

n-Butyl methyl ether is an isomer of MTBE and has a boiling point of 70 oC. Explain why the boiling point is significantly different compared to MTBE.

Draw the structure of each alkene of molecular formula C7H14 that has a tetrasubstituted double bond

Aniline, phenol, and cyclohexanol are all three examples of aromatic hydrocarbons. T/F?

a) Ortho and para have an existing substituent group that produces destabilized resonance for the intermediate carbocation, while in the case of meta, the existing substituent group has stabilized resonance structure(s) for the intermediate carbocation. b) Ortho and para have an existing substituent group that produces stabilized resonance for the intermediate carbocation, while in the case of meta, the existing substituent group has no stabilized resonance structure(s) for the intermediate carbocation. c) Ortho and para have an existing substituent group that produces stabilized resonance for the intermediate carbocation, while in the case of meta, the existing substituent group has destabilized resonance structure(s) for the intermediate carbocation. d) Ortho and para have an existing substituent group that produces stabilized resonance for the intermediate carbocation, while in the case of meta, the existing substituent group has stabilized resonance structure(s) for the…

Which of the following chemical equations depicts an alkylation reaction? C6H6() + CH3Cl() → C6H5CH3() + HCl(g) 2 CH3OH() + 3 O2(g) → 2 CO2(g) + 4 H2O() C6H12() → C6H10() + H2(g) CH2ClCH2Cl(g) + H2(g) → CH3CH3(g) + Cl2(g) CHClCHCl(g) → CH2ClCH2Cl(g)

Markovnikov's rule can best be explained by considering *   a) the number of hydrogen atoms attached to each of the double bond carbons atoms.   b) the number of alkyl groups attached to each of the double bond carbons atoms.   c) the relative stabilities of the carbocations that can be formed from the alkene.   d) the spatial arrangement of the groups around the double bond.   e) All of the above are good explanations for Markovnikov's rule.