2. Predict the order of reactivity being the fastest, 4 being the slowest of primary, secondary...
2) Predict the order of reactivity (1=least, 4=most) of primary, secondary, tertiary, and aryl halides toward nucleophilic displacement by an SN1 reaction mechanism. Explain 3) Give a detailed summary of the chemistry in both reactions SN2 and SN1 in details please for both reactions. include any general statements about the experiments. LAB)o Organic Chemistry I Lab CHEM 3512 Nueleophilic Substitution Reactions: Sl vs S2 To review Sul, S2, El and E2 reactions and mechanisms and compare and contrast the effect...
Experiment F. Nucleophilic Substitution Reactions. Pre -Lab Report 2. SPECIAL INSTRUCTIONS: a. Work in groups of 2-3 students. Each group will complete and turn in one report for grade. You will not complete the lab report in your lab notebook using the usual format. Instead, the entire report is provided in the procedures section of these lab materials. You will complete the report by providing the missing information. Report is due at the end of the lab period. b. While...
Arrange the following in order of decreasing reactivity (fastest to slowest) toward electrophilic aromatic substitution: Arrange the following in order of decreasing reactivity (fastest to slowest) toward electrophilic aromatic substitution: COOH бо ob 6
Rank (slowest to fastest) the following compounds in order of reactivity with respect to an SN2 reaction. Explain your reasoning for the ranking you propose. The compounds are 1-bromo-3-methylbutane, 1-bromo-2,2-dimethylpropane and 2-bromo-2-methylbutane.
1. Compare the reactivity of primary alkyl halides in part 1 (SN2) of this experiment to the reactivity of primary alkyl halides today. What conclusions, if any, can you make about the reactivity of these molecules under these different conditions? Use specific data to make your point. 2. Compare the reactivity of secondary alkyl halides in part 1 (SN2) of this experiment to the reactivity of secondary alkyl halides today. What conclusions, if any, can you make about the reactivity...
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
5. Rank the reactivity of the following alkyl halides (A-E) for an SN2 reaction from the fastest (1) to the slowest (5) and explain your ranking. (10 pts) H3C-Br Br Ci
Rank the reactivity of the following toward H_2SO_4/delta catalyzed dehydration, from 1 (fastest) to 4 (slowest).
rank the organic chlorides from fastest to slowest based on the expected relative reactivity REACTION • The reaction between the four organic chlorides (given below) and a 1% ethanolic silver nitrate solution. HNO, R-CI + AgNO3 + CH3CH2OH Alkyl chloride 2.5 mL 2.0 mL R-OCH CH3 + AgCl + precipitate Alkyl chloride = Alkyl chloride = ra o u to
2. Classify the following alkyl halides as primary, secondary, or tertiary. Which one of these options would be best suited for a unimolecular nucleophilic substitution reaction? مو لہ کی لہ لا 3. Describe the following reactions in written form, making sure to use the following terms where appropriate: nucleophile, lone pair, loss of leaving group, electron-deficient, and electrophile. . و ». . که ملیہ -- « -