label the slowest to fastest e2 reaction time.
2-chloro-2-methylbutene
1-chlorobutane
chlormethane
2-chlorobutene
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label the slowest to fastest e2 reaction time. 2-chloro-2-methylbutene 1-chlorobutane chlormethane 2-chlorobutene
Rank the Sn1 reaction rates for the following compounds: fastest rate 2-chloro-3-methylpentane 3-chloro-3-methylpentane 1-chloro-3-methylpentane chloromethane slowest rate
Rank the following speeds from fastest to slowest. (Label the fastest as 1) 100.3 mi/hr 132.8 km/hr 0.0283 km/s 28.3 m/s
need help with part c and d L euly butane 2-chloro-2-methylbutane 2-chloro-3-methylbutane 2-chlorobutane c) Draw a curved-arrow mechanism for the following reaction: - H2O Hạº, d) Label the following reactions as S1, S2, E1, E2, addition, or acid/base (2 pts, cach). i. Bromoethane becomes ethanol upon treatment with hydroxide ion. ii. 1-Methyl-1-cyclohexanol reacts with acid in water to form l-methylcyclohexene. iii. Propyne becomes propane in the presence of hydrogen and metal catalyst. iv. I-iodopropane reacts with potassium tert-butoxide. SN e)...
Relative ranking (#1 - #7) Reason for ranking 1-chlorobutane 1-chloro-2-butene 2-chlorobutane 1-bromobutane 2-chloro-2-methylpropane bromobenzene benzyl chloride (2) What mechanism do you believe will be favored with AgNO3 in ethanol? What order of reactivity do you predict will be observed when each of the alkyl halides in Figure 1is reacted with AgNOs in ethanol? Complete a similar table as in question #1 for these reaction conditions. Write your prediction of the mechanism and the order of reactivity with AGNO3 in ethanol...
Which of the following alkyl halides reacts the fastest in an SN2 reaction? A) chloromethane B) 2-chlorobutane C) 1-chlorobutane D) 2-chloro-2-methylpropane
2. Three separate reactions are conducted as outlined below. Reaction 1: 4 drops of 1-chlorobutane in 2 mL of 1% AgNO, in ethanol. Reaction 2: 4 drops of 2-chlorobutane in 2 mL of 1% AgNO, in ethanol. Reaction 3:4 drops of t-butyl chloride in 2 mL of 1% AgNO, in ethanol. a. List the expected rate of each of the reactions. List the slowest reaction first and fastest reaction last. b. Explain your reasoning based on substrate structure, the nature...
What is the order of reactivity from fastest to slowest in an SN 2 reaction for the following substrates? t-butyl bromide - A ethyl bromide isopropyl bromide methyl bromide
che 1. Rank from fastest (1) to slowest (5) the rates of the SN2 reaction of the compounds shown. Br Br CH3-C-CH3 CH3 CHaCHs CH2 CH-CH21 CH-CH,он CH3CH2Br 2. Rank from fastest (1) to slowest (5) the rates of the solvolysis reaction in HOAC/HOH of the compounds shown. Br Br CH3-с-CHз CH3CH2OH CH2-CH-CH21 CH3-C-CH3 CH3 CH3CH2Br B. Circle the number corresponding to the correct answer. Answer 5. a) What is the principal determinant of reaction order? i. structure of substrate...
Rank the following functions from slowest growing to fastest growing (i.e. fastest to slowest) 1 (constant) log2n (logarithmic) n (linear) n * log2 n (“n log n”) n2 (quadratic)
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...