I need help with questions 2 and 3.
2. SN1 reaction where a first a carbocation formation takes place followed by a nucleophilic attack of H2O to form tertiary alcohol.
3. E1 reaction where a first a carbocation formation takes place, followed by removal of a proton by the base to form an alkene.
I need help with questions 2 and 3. CH 3 CH3 2. In the reaction below,...
CH3 H 2. In the reaction below, what type of reaction occurred? A. E2 - H₃C B. E1 slow step C. 5 2 HC—C—CI- (-CI) D.S 1 CH3 E. None of above Nuc: CH) → H3C—C—OH HC CH
Which of the alkyl halides below will react the fastest in an SN1 reaction? CH3 CH3 CH3 CH H2C H2C H3C-C-I H-C-Br H3C-C-Br H-C-I CH3 CH3 CH3 CH3 CII-C C-C C-C C-C-IIC
Draw the product to the reaction below. 13C-0-HC CH3 + H3C-CH2-OH CH3 about us careers privacy policy Draw the correct product for the reaction below. H3C—C—C— CH2-CH2-CH3 + H, → Draw the product to the reaction below. CH3 C + H₂C-OH CH₃
12. Label the following reactions as El or E2 * 01 - 0 a . CH CH -- A. A =E1; B=E2 B.A=E1; B=E1 C. A E2: B-EI D. A=E2; B-E2 13. Consider the following exothermic E2 reaction. What rate equation would be observed for this reaction CH, CH CH I + KOC(CH3), CH CH CH2 + KI A. rate k[CHCH:CH-1) B. rate=k[CH,CH:CH:1][K OC(CH.)s] C. rate - [CH,CH:CH=1][K OC(CH);]* D. rate=k[CH,CH:CH-1)^[K OC(CH.):] E. There is not enough information given to...
please answer for me all questions 1-20 1) Identify the alkyl halide that reacts the fastest in a Sn2 reaction. A) chloromethane B) 2-chloro-2-methylpropane C) 2-chlorobutane D) 1-chlorobutane 2) Identify the alkyl halide that reacts the fastest in an SN 2 reaction. A) 1-bromopropane B) 1-fluoropropane C) 1-chloropropane D) 1-iodopropane 3) Which of the following alkyl halides gives the slowest SN2 reaction? A) CH3CH2C1 B) Ci CH3CCH2CH3 CH3 C) CH3CHCH2CH3 CH2 CH3CHCHCH3 C1 СН3 4) Which of the following alkyl...
Write the correct name for each compound below. H3C-CH3: H3C-CH2-CH2-CH2-CH2-CH2-CH2-CH=CH2: H-C≡C-H: H-C-(CH3)3: H3C-CH=CH-CH3:
Draw the product to the reaction below: -CH3-CH2 CH3 + i H3C—C—HC CH3 + CH3 H3C—CH2-OH CH3
alexis Naming Hydrocarbons Compatibility Mode Review View Help Mailings References Layout 1 I 2 3 Naming Worksheet - Hydrocarbons Name: Name of compound H,с- CH CH сH, 1 CH2 CH3 Нас Сн CH 2. Нас нас Methylcyclohexane 3. CHз I Br 4. Hас-нс -сн>-CH-CH, Н.с -сн CH3 -CHз 5. Н.с — сн — с CH3 H3C-CH-CHECH-CH2 CH3 6 но 7. Нс с сн 8 DFocus он DELL O co 6 1 Нас - CH2 CH3 C-CH3 CH3 H3C-CH2-CHECH-CH2 CH3 5....
CHEM 2123/Pre-Lab Study Questions /Exp. #6 Reactivities of Alkyl Halides in Nucleophilic Subs. Reactions Amonda salas Name 1. Classify the following substrates as 1°, 2, 3, aryl, allylic, or benzy lic: CH OCH CHB сна 2. Identify the substrate, nucleophile/base, and the leaving group in the following reactions and indicate the type of reaction (i.e. SN1, SN2, EI, E2) taking place: Br Nal Accionc H.с н.с Нас, CH,OH HEAT сH,он CH-Br Н-о CH CHs CH,CH-ONa HEAT Нс CH3 3. Rank...
2 problems REVIEW Topics [References) CH HC OCH Br2 CH3 B H3C CH,OH H₂C CH₂ Electrophilic addition of hypohalous acids to alkenes yields a 1,2-haloalcohol called a halohydrin. Halohydrin formation, however, does not result from the addition of HOBr, for example. Instead the addition is done indirectly by reaction of the alkene with Br, in the presence of water. The reaction also works with Cl2 to give chlorohydrins instead of bromohydrins. The reaction proceeds through a cyclic intermediate known as...