If a carbon atom has attached to four different groups , the carbon atom is called chiral centre or asymmetric centre
Therefore,
compounds having asymmetric centre are
Which of the following compounds have an asymmetric center? Check all that apply. CH,CH, CHCH CH, CH CHCH...
Part A Which of the following compounds can exist as enantiomers? Check all that apply. CHỊCH CCH2CH2CH3 CH,CH,CHCH OH CH,CH,SH CHS CH3CH, CH CH CH, CH, CHCH.CH СНs CH=CHCHCH: NH Submit Request Answer
Which of the following compounds has one or more asymmetric centers? Check all that apply. ロロロロロ
Part A Which of the following compounds are soluble in water? Check all that apply. "CH₂– CH₂ – C CH3-CH2-OH CH-CH2-CH2-C-0 Na Submit Previous Are Receta X Incorrect; Try Again: 2 attempts remaining Provide feedback Type here to search O et QWERTYliu
CH₂=CHCH₂COOCH₃Check all that apply.alkenearomaticaldehydeesterketoneacid chloridecarboxylic acidaminealkyl halidealkynealcoholetheramidenitrile
Sort enantiomers for each of the following using Fischer projections. Drag the appropriate items to their respective bins. Reset Help H- OH CHỊCH CÀ CHỊ || CHG 1 CHỊCHỤC. CH, CH, HBHHBH-CHHO-H CH.CH CH,OH | CH OH CH,CH, CH(CH), CH(CH), CH, CH CH, CHCHCH CHI,CHCH,OH CICH,CH,CHCH.CH OH
в снення consider the following compounds - CHCH.CH c) CECH - CH(CH) CH-CHCH о снено. Вон CH(CH),CIN hộ CH (CHAN CHAìa а) синон D CH.CH.CH. ENCH-CH2CH3) CH.CH CH(CH2), COCH K) CH.CH OH Which one(s) of the above would be soluble in water? Which one(s) would not be soluble in water but would be soluble in 5% HCI? Which one(s) would not be soluble in water but would be soluble in 5% NaOH? Which one(s) would not be soluble in water...
Which of the reagents listed below would efficiently accomplish the transformation of CH,CH,CH=CHCH,CH,CHO into CHỊCH,CH,CH,CH,CH,CH,OH? 4 Select one or more: Va. KMnO b. NaBH, c. Br in CCIA d. H. Ni Ve. Two of these choices
OCH.CH CH,CH,CHCH, + CH,CH,OH CH,CH,CHCH, + 1 In the above reaction, which of the following is the nucleophile? OOH O CH CH CHCH Or OCH CH OH OCH,CH,0
72 Laboratory 6 Organic Functional Group Tests 9. Complete the following equations: a. CH,COOH + H,0 + b, CHỊCH,NH, + HO © CHỊCH,CHỊCH,CHẠCH-COOH NaOH d. C,H-COOH + NaOH e. C,H-NH, + HCI f. CH,OH + (Ce(NO) g. CH,CHBr + AgNO, h. CH,COO Ag + HNO, → i. CH,CHO + [Ce(NO3) + j. (CH), CHCHO + HN-NH-C,H,(NO), (2,4-DNPH) k (CH),CHCHO + 2 [Ag(NH,),]* + 20H 1. CH,CH,CH=CHCH,CH, + Br, → m. (CH),C=O + H2N-NH-C,H,(NO), (2,4-DNPH) n. cyclohexane + Br-
Question 11 (1 point) CH,CHCH-CHAI CHS CHCHCH,CH SCH3 + 1 CH,OH CH, CH Which of the following would increase the rate of the above reaction? IL Increase the concentration of alkyl iodide. Change the solvent to DMF (shown at right). N(CH3)2 H Il only I only Neither I or 11 Both 1 and 11