Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 9.8, Problem 11P
Interpretation Introduction
Interpretation:
Starting from propyne and using an alkyl halide and other reagents needed, how cis-2-butene can be prepared is to be stated.
Concept introduction:
To state:
Starting from propyne using an alkyl halide and other reagents needed, how cis-2-butene can be prepared.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
How do you synthesize a cyclohexane-1,2,3-triol from a cyclohexane
The pictured reaction shows an alkyl bromide being converted into an alkene.
Choose all reagents that would produce the pictured alkene as the major product.
A) NaOH/H2O
B) H2O
C) tBuOK/tBuOH
D) EtONa/EtOH
5) Determine reaction conditions needed for a multiple step synthesis to transform the starting
material into the product. Show the product after each step (but you do not need to show reactive
intermediates or mechanisms).
OH
Chapter 9 Solutions
Organic Chemistry
Ch. 9.1 - Prob. 1PCh. 9.1 - Prob. 2PCh. 9.3 - What products would you expect from the following...Ch. 9.4 - Prob. 4PCh. 9.4 - Prob. 5PCh. 9.4 - Prob. 6PCh. 9.4 - Prob. 7PCh. 9.5 - Using any alkyne needed, how would you prepare the...Ch. 9.7 - The pKa of acetone, CH3COCH3, is 19.3. Which of...Ch. 9.8 - Prob. 10P
Ch. 9.8 - Prob. 11PCh. 9.9 - Show the terminal alkyne and alkyl halide from...Ch. 9.9 - Beginning with acetylene and any alkyl halide...Ch. 9.SE - Name the following alkynes, and predict the...Ch. 9.SE - From what alkyne might each of the following...Ch. 9.SE - Prob. 16VCCh. 9.SE - The following cycloalkyne is too unstable to...Ch. 9.SE - Prob. 18MPCh. 9.SE - Assuming that strong acids add to alkynes in the...Ch. 9.SE - Prob. 20MPCh. 9.SE - Prob. 21MPCh. 9.SE - Prob. 22MPCh. 9.SE - Prob. 23MPCh. 9.SE - Prob. 24MPCh. 9.SE - Reaction of acetone with D3O+ yields...Ch. 9.SE - Give IUPAC names for the following compounds:Ch. 9.SE - Draw structures corresponding to the following...Ch. 9.SE - Prob. 28APCh. 9.SE - Prob. 29APCh. 9.SE - Prob. 30APCh. 9.SE - Predict the products from reaction of l-hexyne...Ch. 9.SE - Prob. 32APCh. 9.SE - Prob. 33APCh. 9.SE - Propose structures for hydrocarbons that give the...Ch. 9.SE - Identify the reagents a-c in the following scheme:Ch. 9.SE - Prob. 36APCh. 9.SE - Prob. 37APCh. 9.SE - Prob. 38APCh. 9.SE - How would you carry out the following...Ch. 9.SE - Prob. 40APCh. 9.SE - Synthesize the following compounds using 1-butyne...Ch. 9.SE - Prob. 42APCh. 9.SE - Prob. 43APCh. 9.SE - Prob. 44APCh. 9.SE - Prob. 45APCh. 9.SE - A hydrocarbon of unknown structure has the formula...Ch. 9.SE - Compound A(C9H12) absorbed 3 equivalents of H2 on...Ch. 9.SE - Hydrocarbon A has the formula C12H8. It absorbs 8...Ch. 9.SE - Occasionally, a chemist might need to invert the...Ch. 9.SE - Prob. 50APCh. 9.SE - Prob. 51APCh. 9.SE - Prob. 52APCh. 9.SE - Prob. 53APCh. 9.SE - Prob. 54APCh. 9.SE - Prob. 55APCh. 9.SE - Prob. 56APCh. 9.SE - Prob. 57AP
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Draw a detailed, step-wise mechanism for the reaction shown below. SHOW ALL BOND-FORMING AND BOND-BREAKING STEPS. SHOW ALL INTERMEDIATES. 1) NaOH 2) H3O* H3C H3C HOarrow_forward1a). Plan a synthesis of 3,4-dibromoaniline, starting from benzene. 4steps are required, lists reagents needed and draw in the intermediates.arrow_forward3. Complete the following reactions - draw the reactants and products, show the mechanism and conditions, and name the products. These reactions are one step. a) 2-Propanol + butanol → b) Ethanol + [O] → c) Butanone + [H] → d) 2-pentene + H₂O → e) Ethene + H₂ →→ f) Pentanol + HCI → g) Methanoic acid + 2-butanol → h) aminoethane + hexanoic acid → i) Benzene + chloroethane →→ j) Octane + O₂ → 2arrow_forward
- Complete synthesis, show reagents and intermediate compounds.arrow_forwardSynthesis Using reactions we have studied up to this point, propose a multistep synthesis to make the product from the starting material. You will need 3-4 steps.arrow_forwardi) How could you synthesize dipropyl ether from propan-1-ol, TcCl and any other inorganic reagents? Draw the synthetic scheme (likely 2-3 steps) ii) Draw what organic side product might you see from this reaction?arrow_forward
- Synthesize m-chlorophenol from benzene.arrow_forward3. Why do the following two reactions not proceed under basic conditions? Draw the mechanism of each up until the point of failure under basic conditions. HO * OH 4 basic conditions HN Ph * basic conditionsarrow_forwardHow to synthesize 1-methylcyclohexene from cyclohexanone?arrow_forward
- Describe how 1-ethylcyclohexanol can be prepared from cyclohexane. You can use any inorganic reagents, any solvents, and any organic reagents as long as they contain no more than two carbons.arrow_forwardCan you please tell me the reagents/conditions of each step 1, 2, 3 and possible occuring problems (for example: side reaction)? If there's any issues, please explain why the step works well.arrow_forwardAlcohols undergo an oxidation reaction to yield carbonyl compounds on treatment with CrO3. For example, 2-tert-butylcyclohexanol gives 2-tert-butylcyclohexanone. If axial OH groups are generally more reactive than their equatorial isomers, which do you think reacts faster, the cis isomer of 2-tert-butylcyclohexanol or the trans isomer? Explain.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning