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draw 6 acyclic constitutional isomers of C6H12. Provide a name for each isomer, inclduing E-,Z-,R,S where appropriate
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- Rings + Unsaturation --- Hydrogenation If compound A C51H81BrN5O3P3 is hydrogenated to give compound B C51H101BrN5O3P3. How many rings does compound A have? Assume that P has a valency of 5. Would the answer be 4 rings? Formula -> unsat + rings = 1+C +N/2 - H/2 - X/2IQ3 نقطة واحدة Name the following heterocyclic ethers (a) إجابتك نقطة واحدة Name the following heterocyclic ethers H. CH,CH3 (d) CH,CH, H. إجابتك نقطة واحدة Name the following heterocyclic ethers -CH3 CH; () Br إجابتك. II >2. Name the following alkenes: (a) (d) H H₂C C=C CH3 CHCH₂ CH3 H H c=c H3C H₂C=CHCHCH H 17 CH3 CH3 (b) (e) CH3 CH3CHCH₂CH₂CH H3C CH₂CH3 CH3CH₂CH₂ H₂C H C=C C=C C=C CH3 CH3 H H CH3 (c) CH₂ CH3 H₂C=CCH₂ CH3 (f) H₂C=C=CH CH3
- Draw all of the products, both constitutional isomers and stereoisomers, of the following reactions. a) 4,4-dibromo-1-ethylcyclopentene ---->Br2,H2O b) 3,3-dibromo-1-ethylcyclopentene ----> HBr c) 3,3-dibromo-1,2-dimethylcyclopentene ----> 1. BH3. 2. H2O2, NaOH1. Name the following alkenes: H H CH3 CH2CH3 CH3 CH3CHCH2CH2CH H3C C=C H3C CH3 CH3 H2C=CHCHCH CH,CHẠCH2 CH3 H3C CH3 (b)Rank the following alkenes in order of increasing stability: CH,=C(CH3)CH,CH3, CH2=CHCH(CH3)2, and (CH3),C=CHCH3.
- Identify compound Y? Ha Br2 CH3- -CH3 Y Lindlar Pd 2-bromobutane meso-2,3-dibromobutane racemic (2R,3R) and (2S,3S)-2,3-dibromobutane 2,3-dibromo-2-butene Туре: МCQ2 Give the stereochemical relationships between each pair of structures. Examples are same compound, structural isomers, enantiomers, diastereomers. markSI CH, CH, (h) CH,OH CHOH CH, CH, (a) (e) OH HO- H OH HO H- -OH HO H H OH HO- HO H H OH OH HO- CH, CH, CH, CH, CH, CH,Arrange the substituents in order of decreasing priority when determining E/Z stereochemistry of an alkene (i.e., 1 is the highest priority substituent, 4 is the lowest priority substituent). – NHCH3 II - CH v - OCH3 -CH,CI >
- Addition of HCI to the unsymmetrical alkene below could potentially give rise to two products. C2H5. CC=C: C2H5 CH3 (a) Draw the structures of the two potential carbocation intermediates. (b) State which carbocation is more stable. (c) Draw the structure of the major final product.Dehydrohalogenation of 1-chloro-1-methylcyclopropane affords two alkenes (A and B) as products. Explain why A is the major product despite the fact that it contains the less substituted double bond.TReview 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.