Provide names for each structure below. Be sure to include the cis, trans or E.Z designations where applicable: (12 points) ud: word? weled Bubong
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Q: 2. H₂N- 器 + H3N
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- Which of the following structures represents trans-1,2-dimethylcyclohexane (circle correct answer)?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.( please answer with explantion for both correct and incorrect option ) do both
- using the IUPAC rules name every (all four) molecule.6. Which of the following structures represents trans-1,2-dimethylcyclohexane (circle correct answer)? CH3 .CH3 а. H;C. b. H3C CH3 CH ZCH3 с. CH3 d. H3Cll mobily ? 4:13 PM O 21% O < Homework - carboxylic a... CH3CHCH2CH2CHCH3 CH3CCO2H CH3 (c) .CO2H (d) CH3 CH3CCN CH3 (g) Br (h) CN BRCH2CHCH2CH2CO2H Q2: Draw structures corresponding to the following IUPAC names: (a) cis-1,2-Cyclohexanedicarboxylic acid (b) Heptanedioic acid (c) 2-Hexen-4-ynoic acid (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrile Q3: How could you convert butanoic acid into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert each of the following compounds into butanoic acid? Write each step showing all reagents. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert butanenitrile into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) Butylamine
- Show me the steps to solve this please! 1. (3 pts) For the following molecule, draw the Newman projection in its syn, anti, and gauche conformers about the C3-C4 bond, where C3 is the front carbon in the projection. Anti: Syn: Gauche: 2. (3 points) Draw the following cyclohexanes in their lowest energy chain conformations. он 1 of 2pls helpdraw the following compound Plz do Asap...!
- (subjects 3, 4 & 5) Previous Associate each structure or formula with its degree of unsaturation: rà... Questions about AT ✓Choose... 2 11 1 5 10 6 3 9 О 4 7 HN 8 ereoisomerism C₁1H19OF B C NH O MacBook Air C13H18N2O4 D Next page 수 Question 4 Finish your QPart A Cyclize the following compound. || CH3-CH-CH2-CH2-CH-C-CH2CH3 | OH CH3 Draw the molecule on the canvas by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars.АCTIVITY 1 I. Name the following Hydrocarbons, by using the IUPAC Rules and its common name. A =PARENT CHAIN, B = SUBSTITUENTS, C = NAME. 1. | 2. A. А. B. В. C. C. 3. 4. Br Cl- CI А. A. B. В. C. C.