Devise a synthesis of (Z)-4,4-dimethyl-2-pentene using one of the starting materials and any of the reagents belowusing the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in theremaining unused steps.Starting materialsÇH,HC=C-C-CH,HHC=C-C-CH,CH,HC=CHHC=C-CH,HC=C-CH,CH,HC=C-CH,CH,CH,CH,12346Reagentsa NANH, / NH, ()d iodoethaneg 1-bromo-3-methylbutaneį H2 / Lindlar catalystb N2OH/ H20e 1-bromopropaneh t-butyl bromidek H/ NH, ()c iodomethanef 2-bromopropanei H/ Pd on carbonI Na/ NH, ()Starting materialReagent for step 1Reagent for step 2Reagent for step 3

Answered: Image /qna-images/answer/6c3a2b74-b3e6-4fcc-af94-ca5c06b2b63c.jpg

Devise a synthesis of (Z)-4,4-dimethyl-2-pentene using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps. Starting materials ÇH, HC=C-C-CH, HCEC-C-CH, HC=CH HC=C-CH, HC=C-CH,CH, HC=C-CH,CH,CH,CH, 1 2 3 6 Reagents a NANH, / NH,0 d iodoethane g 1-bromo-3-methylbutane į H/ Lindlar catalyst b NaOH/ H,0 e 1-bromopropane h t-butyl bromide k H/ NH, () c iodomethane f 2-bromopropane i H,/ Pd on carbon I Na / NH,() Starting material Reagent for step 1 Reagent for step 2 Reagent for step 3

Devise a synthesis of (Z)-4,4-dimethyl-2-pentene using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps. Starting materials ÇH, HC=C-C-CH, HCEC-C-CH, HC=CH HC=C-CH, HC=C-CH,CH, HC=C-CH,CH,CH,CH, 1 2 3 6 Reagents a NANH, / NH,0 d iodoethane g 1-bromo-3-methylbutane į H/ Lindlar catalyst b NaOH/ H,0 e 1-bromopropane h t-butyl bromide k H/ NH, () c iodomethane f 2-bromopropane i H,/ Pd on carbon I Na / NH,() Starting material Reagent for step 1 Reagent for step 2 Reagent for step 3

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Devise a synthesis of each of the following compounds. Besidesinorganic reagents, you may use hydrocarbons and halides having ≤ 6C′s, and CH2=CHCOOCH3 as starting materials. Each synthesis must use at least one of the carbon–carbon bond-forming reactions.
10
Aside from the specified main starting material, only the following compounds can be used as sources of the carbon backbone for the target compound: acetaldehyde ethanol propanoic acid acetic acid ethyl bromoacetate propan-1-ol benzene (2E,4E)-hexa-2,4-diene propan-2-ol buta-1,3-diene methanol propan-2-one (acetone) (chloromethyl)benzene (benzyl chloride) 5-methyloxolan-2-one sodium cyanide 1-(chloromethyl)-4-methylbenzene phenylacetaldehyde sodium methoxide diethyl propanedioate (diethyl malonate) piperidine sodium ethoxide There are no restrictions with regards to the use of other reagents such as catalysts, solvents, redox agents, protection/deprotection agents, etc. as long as they will not be used as sources of carbon for the skeleton of the target compound. Design a retrosynthetic map and from it, propose a multi-step synthetic approach for the preparation of the target compound from the specified starting material.…
Give the reagents that should be used to carry out the following synthesis
The following tertiary alkyl bromides undergo an SN1 reaction in aqueous acetone to form the corresponding tertiary alcohols. Rank the alkyl bromidesfrom most reactive to least reactive.
Synthesize the following compound using no organic starting materials other than acetic anhydride, triphenylphosphine, ethyne, and alcohols of four or fewer carbons and any inorganic reagents needed
6
Aside from the specified main starting material, only the following compounds can be used as sources of the carbon backbone for the target compound: acetaldehyde ethanol propanoic acid acetic acid ethyl bromoacetate propan-1-ol benzene (2E,4E)-hexa-2,4-diene propan-2-ol buta-1,3-diene methanol propan-2-one (acetone) (chloromethyl)benzene (benzyl chloride) 5-methyloxolan-2-one sodium cyanide 1-(chloromethyl)-4-methylbenzene phenylacetaldehyde sodium methoxide diethyl propanedioate (diethyl malonate) piperidine sodium ethoxide There are no restrictions with regards to the use of other reagents such as catalysts, solvents, redox agents, protection/deprotection agents, etc. as long as they will not be used as sources of carbon for the skeleton of the target compound. Design a retrosynthetic map and from it, propose a multi-step synthetic approach for the preparation of the target compound from the specified starting material.…
Give a synthesis for the following molecules. You can use any isomer of butene, C4H8, as a starting material. HOCH, H CƠ H H Br H Br
The following tertiary alkyl bromides undergo an SN1 reaction in aqueous acetone to form the corresponding tertiary alcohols. Rank the alkyl bromides from most reactive to least reactive.
Draw the structure of the starting material needed to make 2-methylhept-3-yne using sodium amide in liquid ammonia, followed by 1-bromopropane. The starting hydrocarbon must have no more than five carbons 1) NaNH2, NH3() NaBr + 2) CHзCH2CH2Br