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Q: -N(CH CH2)2 + +
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Q: CH2 CH3 (h) CH3 (i) (j)
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Q: а. H;C. CH3 + Br2 b. Cl,
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A: IUPAC nomenclature
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A: The given structure is; CH3O- (methoxide ion) is a strong base.
Q: |Br_Br H-C-C-H Br Br. a. о он 2 KMпO + ЗН-С-СH-CH + 2КОН +. b. CH:CH=CH-CH3 + + 4H2O _+ 2MNO2 С.
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Q: C OD. O B. OC. CH3 A Br CH₂ B AC... CH3 CH₂ Br H3C Br C CH₂ معاكم
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Q: A) CH,),CCO(CH,),CH3 C) A
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Q: CH3 H.C OH KMnO4 H₂C CH3 H ->>
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Q: CH3 H* CH3 H3C OH
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A: Applying concept of stereochemistry.
Q: Give a clear handwritten answer and explain
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Q: CH3 b) CH3 HO Br Br OH c) H3C NH H3C d) CH3
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- Indicate the product of each reaction belowThe stereochemistry of the products of reduction depends on the reagent used, with this in mind, how would you convert 3,3-dimethylbutan-2-one [CH3COC(CH3)3] to: (a) racemic 3,3-dimethylbutan-2-ol [CH3CH(OH)C(CH3)3]; (b) only (R)-3,3- dimethylbutan-2-ol; (c) only (S)-3,3-dimethylbutan-2-ol?(CH3)3CCH=CHCl (1)NaNH2 -----> (2)H2O Which of the following is the product for the given reaction? a) (CH3)3CCH≡CH b) (CH3)3CCH=CH2 c) (CH3)3CCH=CHOH d) (CH3)3CCH=CHNH2
- Which substituent is the strongest deactivator to EAS reactions? -NO2 -Cl -CH3 -OHWhat is the major product of the following reaction sequence?Tek seçenek.What is the major organic product of the SN1 reaction shown? (CH3)2CHCH(OH)CH2CH2CH3+HBr⟶ The product is: a. CH3CHBrCH(CH3)CH2CH2CH3 b. (CH3)2CHCH2CHBrCH2CH3 c. (CH3)2CBrCH2CH2CH2CH3 d. (CH3)2CHCHBrCH2CH2CH3
- Which keto product would be isolated from the reaction shown? A B C D EDraw the products formed when (CH3)2C=CH2 is treated with each reagent.a. HBrb. H2OH2SO4c. CH3CH2OH, H2SO4d. Cl2e. Br2, H2Of. NBS (aqueous DMSO)g. [1]BH3;[2]H2O2, HO-Draw the favored product(s) of the following reactions (organic chemistry)
- Draw the product formed when CH3CH2C=CH is treated with each of the following sets of reagents: (a) H2O, H2SO4, HgSO4; and (b) R2BH, followed by H2O2, HO−.Which set of reagents are most likely to affect the E2 elimination? a. CH3CH2O-, CH3CH2OH b. (CH3)3CO-, (CH3)3COHDraw the substitution product formed (including stereochemistry) when (R)-hexan-2-ol is treated with each series of reagents: (a) NaH, followed by CH3I; (b) TsCl and pyridine, followed by NaOCH3; (c) PBr3, followed by NaOCH3. Which two routes produce identical products?