Question 4 Rank these alkenes as to stability: CH3 H&C H3C A OA most, C least OC most, B least OA most, B least OC most, A least OB most, A least OB most, C least B CH3 CH3
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![Question 4
Rank these alkenes as to stability:
CH3
H&C
H3C
A
OA most, C least
OC most, B least
OA most, B least
OC most, A least
OB most, A least
OB most, C least
B
CH3
CH3](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fce99da84-d312-4267-b001-b85941710d4a%2Fde2b4135-3a77-44a7-bcc6-98d88c00b016%2Fcx9mmk9_processed.jpeg&w=3840&q=75)
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- H Cl prs OH Et3N H Draw the molecule on the canvas by choosing buttons from the Tools (for bonds and charges), Atoms appropriate stereochemistry by choosing the dashed or wedged buttons and then clicking a bond ons® Give the IUPAC names of the following alkyl halides: ÇI CH3 CH;CH,CHCHCH3 la) Br (bl (c) CH3 CH;CH;CHCH3 CH;CHCH;CH,CI ÇI (al BrCH,CH;CH,CH2CI If) Br CH3CCH2CH;CI CH3CHCH,CH,CH2CI ČH3TReview TOpics] [References Draw a structural formula for the major product of the reaction shown. CH3 CH3CHCH=CH2 Show product steréochemistry IF the reactant alkene has both carbons of the double bond within a • Do not show stereochemistry in other cases. If the reaction produces a racemic mixture, just draw one stereoisomer. C P opy aste C.
- Nonehow to name these heterocyclics? please show the steps to name each compound8. Which of the following compounds are correctly classified as isomers of each other? A) CH3CH2CH2-NH2 B) CH3-NH-CH2CH3 c) CH;-N-CH3 CH,CH-NH, ČH; D) O a. only A and B O b. only A, B and C O c. only A and C Od. all four are isomers
- I arther: Chair conformers Monosubstituted rings The A-value for methyl, ethyl, isopropyl, and t-butyl substitution on a cyclohexane ring are 7.1kJ/mol, 7.3 kJ/mol, 9.0kJ/mol, and 18.8 kJ/mol, respectively.. Me Me 1. Et 95:5 95:5 Bu Bu 97:3 9995:5 Build the molecules and use your model to explain why the increased size of the substituent doe- not have a dramatic effect until you reach t-butyl. In other words, is it possible for the first three substituents (methyl, ethyl, and isopropyl) to achieve conformation in which 1,3-diaxial interactions are minimized? mlugiest bn todte has -value: 0 9k.J/mol. Build the molecule in order to deterrone 4Pd (CH, CH,),N organohalogen alkene2) Which term best describes the alkene below? F F A) cis only B) trans only C) both terms may be used D) neither cis nor trans
- the energy diagrmm for the general reaetrin of a Smmple älkane witn HBR would shoiw? a) two Steps and one ntermedate A) dues Steps and po prlemeliale one Step and one Mtermedale a)ene Step and no mtermediateDraw the organic product of the following reaction. CH3 m-CICgH,CO;H • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, just draw one stereoisomer. • If more than one product is possible, only draw the major product. opy asteConsider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.
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