Identify the structure of 3-phenylpentane 1 ΠΙ CHÍCH,CH HẠCH CH a. I IV O > d. II IV. OH СЊСЊ СНСН СН V. How many asymmetric centers are present in the compound shown below? a. 4 Ob 5 Oc 2 d 6 3 (CH3)2 N. Which of the following carbocations is/are likely to rearrange? OH CH3 CCCH3
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- What is(are) the major Organic product(s) in the following reaction? CH; CH; H₂C-C-0-CBr; CBr; CH; H₂C-C-0-CH; CH; CB13 Br3C C 0-CH₂ HBr (SNI) HC CH; H₂C-C-0-H CH, (b) CH; CH; Br CH;Br CH₂OH H;C CH, H₂C C | CH; CH; C CH; (c) H CH + CH₂Br CH; 0—C—CH; -CH:OCH:1. /TSOH Cyclohexanone- B 2. H;C=CHCH;CIWhat is(are) the major organic product(s) of the following reaction? II CH3CO2Na CH;CH2CH2CCI A) CH;CH;CH,COČCH; B) CH;CH,CH,CO,Na + CH;CI C) CH;CH¿CH¿COCH3 D) CH;CH2CH,CCH;
- Name each compound in which the benzene ring is best treated as a substituent. a. H;C-CH;-CH-CH-CH,-CH; H;C b. ČH;-CH2-CH;-CH2-C=C-CH, CH3 c. CH;-CH- CH-C=CH-CH-CH2-CH; CH3 CH,The action of heating one mole of water (containing a trace of acid catalyst) on one mole of compound Y produces one mole of CH,COOH and one mole of CH, CH,NH, The structure of Y is: Select one: O CHCNCCH, CH,CH,NHCH,CH, OH CH CHNHCH,CH, O CHCH,CNHCH; O CH;CH NHÖCH;Q2. Provide the reagents O OMe OMe CO₂Me CO₂Me
- Identify the major product of this reaction of an alkene. | ||| OH OH 1. Hg(OAc)2, H2O 2. NaBH4, NaOH || IV ㅊ OH OHName each alkene. c. CH2=CH-CH-CH,-CH2--CH; CH;-CH CH CH; d. CH;-CH-CH=C-CH; CH2-CH,What is the major Organic product of the following reaction? (d) O ZEU OH CH₂N₂ CH; (b) (e) NH₂ NH₂ C (0) OCH, CH;
- 2-propanone is reacted with hydrogen gas and a metal catalyst to produce ОН a. CH;CH=CH, + H,O b. CH;CCH, с. CН CH,ОH - СH d. CH;CHCH;What is the organic product formed in the following reaction? CGHS-CH=CH-ċ-CH; (CH;CH),ÑH II C3H3-CH,-CH- C,Hs-ÇH-CH-C-CH; (CH;CH);Ñ -CHs (CH;CH);Ñ OH IV o-N(CH2CH3), C3H3-CH=CH- -CHs CgHs-CH=CH-Ċ-CH; (CH;CH),N Select one: O A. IV B. II O C.I D. IIWhich of the followings is the principal organic product of the reaction shown below? TsCl= TSCI CH,CH, pyridine as shown below TS0H CH;CH, as shown below CH;CH, as shown below CH-CH, as shown below T50FOTS CH;CH3 as shown below CH,CH,