Select all descriptors that are correct for methylcyclopentane: 5 carbons total 6 carbons total with a carbon-carbon double bond with a carbon-carbon triple bond linear O cyclic
Q: equivalent hydrogens
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- Answer the following Compounds CORRECTLY by giving the IUPAC NAME OF IT. •Label with proper notations (like hyphen, commas, periods, and grouping symbols) thank u❤️Draw all possible constitutional isomers for compound [1]For each of the following substituents, indicate whether it withdraws electrons inductively, donates electrons by hyperconjugation, withdraws electrons by resonance, or donates electrons by resonance. (Effects should be compared with that of a hydrogen; remember that many substituents can be characterized in more than one way.)
- calculate the hydrogen deficiency of each compound c7h10cl2 c10h12n2o c4h3f7o draw a compound for #1Which group is of lower priority than –CH=CH2 according to Cahn-Ingold-Prelog rules. –CH=C(CH3)2 –C(CH3)3 –CH(CH3)2 –CH=CHCl a b c dDraw the structure of all compounds that t the following descriptions.a. ve constitutional isomers having the molecular formula C4H8b. nine constitutional isomers having the molecular formula C7H16c. twelve constitutional isomers having the molecular formula C6H12 and containing one ring
- Draw a line structure for (4E,7S)-7-benzyl-5-fluoronon-4-en-2-one with threedimensional information where appropriate. Place the ketone group on the right-hand side of your drawing.Rank the three compounds below in order of shortest to longest carbon–oxygen bond length and explain your reasoning A)Tetrahydro-2H-pyran-2-one B)cyclohexane C)1-Methyl-2-piperidinoneDraw the skeletal (line-bond) structure of (S)-1-ethoxy-2-methylhexane. Use dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.
- Determine a reasonable molecular formula for a compound with a molecular weightof 113. Show your work. b. Report the degrees of unsaturation for your formula.Draw a skeletal (line-bond) structure of (R)-2,2,3 trimethylhexane. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.Build a model of methylcyclohexane, and use the model to complete the following Newmanprojections of methylcyclohexane in the chair conformation: a. When the methyl group is in an axial or equatorial (circle one) position, the molecule is inits lowest potential energy conformation. b. Label one Newman projection above anti and the other gauche to describe the relationshipbetween the methyl group and C3 of the ring. c. In general, which is a lower PE conformation, anti or gauche? d. Explain how your answer to b and c provide an explanation for why it is more favorable fora large group to be in an equatorial than an axial position.