ORGANIC CHEMISTRY-PRINT (LL)-W/WILEY
4th Edition
ISBN: 9781119761105
Author: Klein
Publisher: WILEY
expand_more
expand_more
format_list_bulleted
Question
Chapter 7.11, Problem 36PTS
(a)
Interpretation Introduction
Interpretation:
The transformation from the given starting material to the target molecule must be shown along with Retrosynthetic analysis.
Concept Introduction :
A Retrosynthetic analysis helps to find out the suitable starting material for a target molecule synthesis. Thioether can be synthesized following
(b)
Interpretation Introduction
Interpretation:
The transformation of the target molecule must be shown along with Retrosynthetic analysis.
Concept Introduction :
A Retrosynthetic analysis helps to find out the suitable starting material for the synthesis of a target molecule. Williamson ether synthesis follows the SN2 pathway in which sodium alkoxide and alkyl halide are used.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Suggest a sequence of reagents that would accomplish this. Suggest a sequence of reagents that will accomplish the following.
Complete the mechanism for the given reaction of 2‑butanone in methanethiol and acid by adding any missing atoms, bonds, charges, nonbonding electrons, and curved arrows. Select the name that best describes the final product.
Show all intermediates, mechanisms, and
reagents. With each synthetic step in a true
synthesis, you would need to analyze your
product and confirm that you had isolated the
correct intermediate or product. Often, a quick
analysis is performed looking for a key signal
that would confirm the desired product and
confirm no starting material remains. For each
step in your synthesis, explain how you would
analyze the product to a) confirm product
formation and b) confirm there is no remaining
starting material. Your answer should clearly
explain which analytical instrument you would
use, what signal(s) you would look for and how
that/those signal(s) would answer these
questions.
Br
OH
OH
OH
Chapter 7 Solutions
ORGANIC CHEMISTRY-PRINT (LL)-W/WILEY
Ch. 7.2 - Prob. 1CCCh. 7.3 - Prob. 2CCCh. 7.3 - Prob. 1LTSCh. 7.3 - Prob. 3PTSCh. 7.3 - Prob. 4ATSCh. 7.3 - Prob. 2LTSCh. 7.3 - Prob. 5PTSCh. 7.3 - Prob. 6ATSCh. 7.3 - Prob. 7CCCh. 7.4 - Prob. 8CC
Ch. 7.5 - Prob. 9CCCh. 7.6 - Prob. 10CCCh. 7.6 - Prob. 11CCCh. 7.7 - Prob. 12PTSCh. 7.7 - Prob. 13PTSCh. 7.7 - Prob. 14ATSCh. 7.7 - Prob. 4LTSCh. 7.7 - Prob. 16ATSCh. 7.7 - Prob. 17CCCh. 7.7 - Prob. 18CCCh. 7.7 - Prob. 5LTSCh. 7.7 - Prob. 19PTSCh. 7.7 - Prob. 20ATSCh. 7.8 - Prob. 21PTSCh. 7.8 - Prob. 22ATSCh. 7.8 - Prob. 23CCCh. 7.8 - Prob. 24CCCh. 7.8 - Prob. 25CCCh. 7.8 - Prob. 26CCCh. 7.8 - Prob. 27CCCh. 7.9 - Prob. 7LTSCh. 7.9 - Prob. 29ATSCh. 7.9 - Prob. 30ATSCh. 7.9 - Prob. 31ATSCh. 7.10 - Prob. 32CCCh. 7.10 - Prob. 33CCCh. 7.10 - Prob. 34CCCh. 7.11 - Prob. 8LTSCh. 7.11 - Prob. 35PTSCh. 7.11 - Prob. 36PTSCh. 7.11 - Prob. 37ATSCh. 7.11 - Prob. 9LTSCh. 7.11 - Prob. 40PTSCh. 7.11 - Prob. 41ATSCh. 7.12 - Prob. 42CCCh. 7.12 - Prob. 43CCCh. 7.12 - Prob. 44CCCh. 7.12 - Prob. 45CCCh. 7.12 - Prob. 46CCCh. 7 - Prob. 47PPCh. 7 - Prob. 48PPCh. 7 - Prob. 49PPCh. 7 - Prob. 50PPCh. 7 - Prob. 51PPCh. 7 - Prob. 52PPCh. 7 - Prob. 53PPCh. 7 - Prob. 54PPCh. 7 - Prob. 55PPCh. 7 - Prob. 56PPCh. 7 - Prob. 57PPCh. 7 - Prob. 58PPCh. 7 - Prob. 59PPCh. 7 - Prob. 60PPCh. 7 - Prob. 61PPCh. 7 - Prob. 64PPCh. 7 - Indicate whether you would use NaOEt or tBuOK to...Ch. 7 - Prob. 68PPCh. 7 - Draw a plausible mechanism for each of the...Ch. 7 - Prob. 70PPCh. 7 - Prob. 71PPCh. 7 - Prob. 72PPCh. 7 - Prob. 73PPCh. 7 - Prob. 74PPCh. 7 - Prob. 77PPCh. 7 - Prob. 78PPCh. 7 - Prob. 81ASPCh. 7 - Prob. 87ASPCh. 7 - Prob. 90ASPCh. 7 - Prob. 91IPCh. 7 - Prob. 92IPCh. 7 - Prob. 93IPCh. 7 - Prob. 94IPCh. 7 - Prob. 95IPCh. 7 - Prob. 96IPCh. 7 - Prob. 97IPCh. 7 - Prob. 98IPCh. 7 - Prob. 99IPCh. 7 - Prob. 100IPCh. 7 - Prob. 101IPCh. 7 - Prob. 102IPCh. 7 - Prob. 103IPCh. 7 - Prob. 105IPCh. 7 - Prob. 106IPCh. 7 - Prob. 107IPCh. 7 - Prob. 109IPCh. 7 - Prob. 110CPCh. 7 - Prob. 112CPCh. 7 - Prob. 114CP
Knowledge Booster
Similar questions
- Select the conditions in which elimination/condensation is most likely to occur. Note that only one of these needs to be present for elimination/condensation to be likely. Protic solvent Aprotic solvent Acidic conditions Basic conditions Cold Hot Shorter reaction time Longer reaction timearrow_forwardShow the complete mechanism for the following transformation.arrow_forwardComplete the mechanism for the formation of the major species at equilibrium for the reaction of butanal in methanol solvent and catalytic aqueous acid. Make sure to include any missing atoms, bonds, charges, nonbonding electrons, and curved arrows.arrow_forward
- Give two possible [1,2]-rearrangement products where an alkyl group migrates in the following compound. Motivate also which of the two products will be formed preferentiallyarrow_forwardSeveral reagents and several organic structures are shown below. Construct a multistep synthetic route for the synthesis of acetylene from ethane by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used. (Stoichiometry is omitted.)arrow_forwardSynthesise the target molecules drawn below using precursor chemicals within the following limitations: 1) ALL intermediates and reagents must be shown.2) Each molecule requires multiple step synthesis.3) You must also synthesize any organometallic reagents or ligands that you wish to use. b) Use any precursor molecules with 7 carbon atoms or less.arrow_forward
- Nonearrow_forwardSeveral reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.arrow_forwardSynthesise the target molecules drawn below using precursor chemicals within the following limitations: 1) ALL intermediates and reagents must be shown.2) Each molecule requires multiple step synthesis.3) You must also synthesize any organometallic reagents or ligands that you wish to use. a) Aspirin is a common pain killer that was developed by Bayer.arrow_forward
- In a Wittig reaction, a ketone or aldehyde reacts as an electrophile with a nucleophile called a Wittig reagent (or phosphonium ylide) to produce an alkene. The Wittig reagent is commonly synthesized first in a two-step process beginning with an alkyl halide, then reacted with the carbonyl compound. In this problem, you'll explore the mechanism of a multi-step synthesis to make an alkene using the Wittig approach.arrow_forwardwhat is a multistep synthesis for this transformation. add any reagents or compounds to help accomplish itarrow_forwardProvide a multi-step synthesis of the "Final Product" from the given "Reactant" by completing the synthesis scheme below. Draw the entire synthesis scheme & complete the synthesis scheme and box your answers as shown below. Indicate the set of reagents/conditions #1, #2, and Draw the chemical structure of major organic product at each step i.e. Compounds A, B, and C. Each set of reagents/conditions may contain more than one reagent. Use the notation 1., 2., etc., to show the steps in each set of reagents/conditions as appropriate. Do not show any curved-arrow pushing mechanisms. (Reactant) Final Product TSOH HO OH Compound A Reagents/Condition(s) #1 Compound B MOTHE Reagent(s)/Condition(s) #2 Compound Carrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning