Question

1. What techniques are the apparatuses below used for? 2. Give the name of the pieces of lab equipment below. 3. Describe refluxing and why it would be necessary to perform during a reaction 4. Give the mechanism of the preparation of n-butyl chloride from n-butanol using hydrobromic acid produce from the reaction of sodium bromide and sulfuric acid. 5. The reaction above primarily undergoes: D. E2 B. SN2 a. SN1. 6. HBr was formed in situ from the reaction of NaBr and Hnso. What does in situ mean?
0 0
Add a comment Improve this question Transcribed image text
Answer #1

5. The preparation of n-butyl chloride from n-butanol using hydrobromic acid produce from the reaction of NaBr and H2SO4 is mainly undergoes SN2 reaction. This is because 1 deg alkyl halide due to less steric crowding prefers SN2 reaction. SN1 is not preferred as the 1 deg carbocation is not sufficient enough to undergo SN1 reaction.

Add a comment
Know the answer?
Add Answer to:
What techniques are the apparatuses below used for? Give the name of the pieces of lab...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • complete #1 and #2 and please explain! Nucleophilic Substitutions: Competing Nucleophiles Dry Lab Name When an...

    complete #1 and #2 and please explain! Nucleophilic Substitutions: Competing Nucleophiles Dry Lab Name When an alcohol (substrate) is placed in an excess equimolar amounts of chloride ions and bromide ions in acid media the corresponding alkyl halides are obtained. The ratio of the alkyl halides depends on several factors: the nature of the substrate, the reaction conditions, the solvent and the mechanism of the reaction. (Refer to your lab textbook, see syllabus schedule) When fert-butanol (density 20 °C-0.7858 g/mL)...

  • What is Zaitsev’s rule? Give the mechanism for the acid-catalyzed E1 reaction of 2-butanol. Give the...

    What is Zaitsev’s rule? Give the mechanism for the acid-catalyzed E1 reaction of 2-butanol. Give the mechanism for the base-catalyzed E2 reaction of 2-bromobutane. Draw all possible products. You expect three products from the elimination reaction 2-butanol. What are they? The E2 mechanism is a one-step mechanism. True or False? Explain. Which of these two alcohols would you expect to be more reactive under H3PO4/aqueous conditions? Why? Give the structure of the main product in both cases. 1-phenyl-1-propanol 1 -cyclohexyl-1-propanol...

  • how do I get the molar ratios between NaBr, 1-butanol and H2SO4 used in the experiment...

    how do I get the molar ratios between NaBr, 1-butanol and H2SO4 used in the experiment sn2 reaction 1-bromobutane Moles: NaBr: 0.0275 Butanol: 0.0216 H2SO4: 0.00840 butanol is the limiting reagent Experiment: 08 The S2 Reaction: 1-Bromobutane Substitution nucleophilic bimolecular (SN2) reactions can be utilized to convert primary alcohols to corresponding halogens. In this experiment, 1-butanol is treated with a nucleophile (Br) to generate the corresponding 1-bromobutane. The nucleophile in this lab is generated from an aqueous solution of NaBr....

  • 1.1 In which of the following solvents would the reaction of 1-bromobutane with sodium azide,NaN3, proceed...

    1.1 In which of the following solvents would the reaction of 1-bromobutane with sodium azide,NaN3, proceed the fastest? a.aceticacid b.ethanol c.water d.acetonitrile 1.2 Which of the following solvents is the best choice for the reaction of 1-chlorohexane with sodium bromide? a.dimethylsulfoxide b.water c.hexane d.toluene,PhCH3 1.3 Which of the following is most likely to undergo rearrangement during reaction with methanol? 1.4 Name which energy diagrams represents the course of an exothermic SN1, SN2,E1, or E2 reaction? 1.5 Which of the following...

  • Questions 2-10 please!! 1) A substitution reaction is: [2] a) A reaction during which an OH...

    Questions 2-10 please!! 1) A substitution reaction is: [2] a) A reaction during which an OH group of a molecule is replaced by a halogen. b) A reaction during which water is the leaving group. c) A reaction during which a functional group of a molecule is replaced by an electrophile. d) A reaction during which a functional group of a molecule is replaced by another functional group. V 12 2) Substitution reactions are classified either as electrophilic or nucleophilic...

  • [Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl...

    [Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl groups are isopropyl, isobutyl, sec-butyl, and tert-butyl. CH2CH3 CH3CH2CH2CCH2CH3 Submit Answer Retry Entire Group 9 more group attempts remaining The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Br NaOCCH, . CH3CH2CHCH 1. none h. HBr 1.H20 e. "CCH3 f. Br j. Nat 9. HOCCH3 k. "OCCH3 Which letter designates the electrophilic carbon at which substitution occurs? (If no...

  • Synthesis of 1-Bromobutane: An SN2 Reaction Pre-Laboratory Exercises PRE-LABORATORY EXERCISES NAME: Cynthesis of 1-Bromobutane: An SN...

    Synthesis of 1-Bromobutane: An SN2 Reaction Pre-Laboratory Exercises PRE-LABORATORY EXERCISES NAME: Cynthesis of 1-Bromobutane: An SN 2 Reaction Butylbromide was prepared by refluxing in a 100-ml round bottomed flask a solution containing 13:35 Br 15 ml of water, 10 mL of n-butyl alcohol. 15 ml of concentrated H.SO. and a few boiling stories, 1. 2. R." d 1.275 laborales Nel CH3CH2CH2CH2OH + NaBr H2SO4 Superletalyst CHCH2CH2CHBr + NaHSO + HO (eq. 16) 1-butanol bp 118 C 1-bromobutane d 0.810 bp...

  • please help with how the flow chart will look like? thank you! Synthesis of n-Butyl Bromide...

    please help with how the flow chart will look like? thank you! Synthesis of n-Butyl Bromide Purpose of the Experiment: In this week's experiment you will be synthesizing n-butylbromide (IUPAC 1-bromobutane from 1-butanol and a concentrated acid via a nucleophilie substitution reaction. It is important to know that alcohols dehydrate to form alkenes in the presence of strong inorganic acids, so care must be taken in this experiment not to heat the reaction too vigorously else an elimination reaction may...

  • 24. What would have been the effect of omitting the sulfuric acid from methyl benzoate preparation...

    24. What would have been the effect of omitting the sulfuric acid from methyl benzoate preparation by reacting benzoic acid with methanol? 25. Criticize the following techniques: (a) Heating a mixture that contains n-hexane using an open flame. (b) For a reaction, heating a mixture that contains a large amount of toluene using hot water bath. (c) Running s reaction with tert-butyl alcohol that is cooled to 0°C in an ice bath. (d) A 100-ml graduated cylinder is used to...

  • Tab Caps Loc Postlab Exercises Record all data during the experiment in your the lab notebook. When the lab is comp...

    Tab Caps Loc Postlab Exercises Record all data during the experiment in your the lab notebook. When the lab is complete Summarize your results on this sheet and tum it in, along with the copy sheets from your notcbook Shitt 1 Ctri Synthesis Results (show all calculations in lab notebook) 0-D459 moles 0,0534 moles 0.01 (3 moles 1-Pentanol mass 5.50q 2.019 Sodium bromide mass 1-Bromopentane massi Theoretical yield mass 49.l631 % Yield Postlab Questions Give your answers and calculations on...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT