7. For the two reactions below show the mechanism and mention the type of substitution or...
Classify each of the following organic reactions. Substitution Addition Elimination Type of Reaction Reaction CH3 CH3 CH3-CH=C-CH3 + H20 – CH3-CH2-C-CH3 OH CH3-CH2-CH=CH2 + HCI → CH3-CH2-CH-CH3 CI CH3-CH-CH2-CH3 + CH3-CH=CH-CH3 + HBr Br
Classify each of the following organic reactions. Substitution Elimination Addition Type of Reaction Reaction CH3-CH2-CH2-CH3 + Cl2 → CH2-CH2-CH2-CH3 + HCI CI CH3-CH=CH-CH3 + Cl2 → CH3-CH-CH-CH3 CICI CH3-CH2-CH-CH3 - CH3-CH2-CH=CH2 + HCI
Classify each of the following organic reactions. Substitution Elimination Addition Type of Reaction Reaction OH CH2-CH + HCN– CH3-CH-CN CH3-CH2-CH2-OH + HBr – CH3-CH2-CH2-Br + H2O CH3-CH=CH-CH3 + HBr – CH3-CH-CH2-CHz Br
8. complete the following reactions. mention the type of
mechanism (SN1,SN2, E1, or E2) that each follows
8. Complete the following reactions. Mention the type of mechanism (SNI, SN2, E1 or E2) that each reaction follows. (4) (CHy)COH 100°C Br a) Cl Xiocn, NaOCH3 Heat CH3 b) Cl CH3ONa CH3OH,100°C CH3
Question 3 [2 Marks] A. Name the following reactions as reduction, oxidation, substitution, elimination reactions. (1 Mark) CH Na/NH, i) Học = | CH - NaNH » H=": Н3С. H3C H2SO4 H3COH - 70°C C H3C CH2 + H2O H3C CH3 heat CH3 CH3 -C-CH3 + HCI- OH CH3-C-CH3 + H2O CH3 CH2 CH3 + 502 — >3CO2 + 4H20
Substitution and Elimination
Reactions: Complete the following mechanism involving
1-iodo-2,2-dimethylpropane.
Substitution and Elimination Reactions: Complete the following mechanism involving 1-iodo-2,2-dimethylpropane. 3 of 3 сH, CH3 Ag - CH Нас- Н,С. Н,о CHa он Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron flow arrows should start on an atom or a bond and should end on an atom, bond, or location where a new bond should be...
8. Complete the following reactions. Mention the type of mechanism (SNI, SN2, El or E2) that each reaction follows. Mention major and minor peoducts.(4) E.2 (CHСОН Br al 100°C E2 NaOCH, Heat CHy b) E I CH,ONa CH ОН, 100°C CHy E I conc. H,SO4 OH d) heat 5
_1. An alkyl halide which might be expected to undergo rearrangement under Snl or E1 conditions is: HZC Br CH3 A. 1 B. | F—CH,BH C. CH3-C-CH-CH, CHz CH3 D. CH3 CH3-C-CH2CH2-Br CH3 E. A Br 2. Your task is to convert 2-chloropentane into 1-pentene. Which reagents would you choose? a) NaOH/H20 b) KOH/CH3OH c) CH3ONa/CH3OH d) CH3CH2ONa/CH3CH2OH e) (CH3)3COK/(CH3)3COH 3. Circle the reaction below which is faster in polar protic solvents. OH,H,O A. CH,CH,CH,Br- CH,CH,CH,OH + Br or SH.RSH...
Substitution Problems I. In each of the problems below, label the alkyl halide as primary, secondary, or tertiary. Label the nucleophile as strong or weak. Decide whether an SN2 or an Sy1 reaction occurs. After, show the mechanism and product or products. Indicate stereochemistry where appropriate. a. Reaction of 1-bromopropane and sodium methoxide in methanol CH3 Na CH,Oн Br b. Reaction of 2-bromopropane in ethanol CH3CH2OH Br c. Reaction of (R) 3-chloro-3-methyl heptane in acetic acid Ci Cн CH,COOH но...
4. Classify each of the following reactions as: Acid/ Base, Addition, Elimination, Reduction, Oxidation, Condensation, or Hydrolysis. (7 points each) a. CH3CH2OH [O] + CH3-CH (H2) [O] P → CH-E-OH (+0) (conc. Acid and heat) b. CH3-CH2-CH2-OH CH3-CH=CH2 + H2O (Pt cat) c. CH3-CH=CH2 + H2 → CH3CH2CH3