You need synthesize cyclopentanone starting with the lactone shown below in 9 steps where 3 of...
You need synthesize cyclopentanone starting with the lactone shown below in 9 steps where 3 of the steps are acid workups.
Note - you should use reagent D three times and there are three other reagents in the table that are not used at all - ALL OTHER ITEMS (but those 3) ARE USED.
Step 1
Step 2
Step 3
Step 4
Step 5
Step 6
Step 7
Step 8
Step 9
STEP 1 is not F (NaOH, heat)
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You need synthesize cyclopentanone starting
with the lactone shown below in 9 steps where 3 of...
You need synthesize cyclopentanone starting with the lactone shown below in 9 steps where 3 of...
You need synthesize cyclopentanone starting
with the lactone shown below in 9 steps where 3 of the steps are
acid workups.
Note - you should use reagent D three times and
there are three other reagents in the table that are not used at
all - ALL OTHER ITEMS (but those 3) ARE USED.
Step 1
Step 2
Step 3
Step 4
Step 5
Step 6
Step 7
Step 8
Step 9
You need synthesize cyclopentanone starting with the lactone shown below in 9 steps where 3 of...
You need synthesize cyclopentanone starting with the lactone shown below in 9 steps where 3 of the steps are acid workups. A LDA B LAH C heat D H30 (aqueous acid) E PCC F NaOH, heat G NaOCH2CH Na Cr207, aq acid H HOCH2CH, acid, heat NBS Note there are 3 reagents on this table that are not used ALL OTHERS ARE USEI
the steps are B,D,H,I,G,D,F,D,C Synthesis You need synthesize cyclopentanone starting with the lactone shown below...
the steps are B,D,H,I,G,D,F,D,C
Synthesis You need synthesize cyclopentanone starting with the lactone shown below in 9 steps where 3 of the steps are acid workups. Cheat DH,O (aqueous acid) E pcc F NaOH, heat G NaOCHCH H Na,Cr,0,.aq acid HOCH,CH,, acid, heat NBS Note- there are 3 reagents on this table that are not used - ALL OTHERS ARE USEI Steps Reaction names Give the name of the type of reaction for each step, (examples: acidification, reduction, saponification decarboxylation,...
Devise a synthesis of (Z)-3-octene using one of the starting materials and any of the reagents...
Devise a synthesis of (Z)-3-octene 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 нсисынсно-си нос-сцен нос-cң соң,он нонс Reagents + NaNH / NH diodo ethane 1-bromo-3-methybutane H undar catalyst + NaOH HẠO e 1-bromopropane butyl bromide күн clodomethane 1 2-bromopropane H/Pd on carbon I N/NH0 Starting material Reagent for step 1...
The reagent options are the same for all boxes Trans-4-hexen-3-ol can be synthesized starting from acetaldehyde....
The
reagent options are the same for all boxes
Trans-4-hexen-3-ol can be synthesized starting from acetaldehyde. One of the key reagents is ethyl grignard. Synthesize ethyl grignard from acetaldehyde in the steps below using the reagents provided. Synthesize (trans)-4-hexen-3-ol from acetaldehyde. Select the best reagents and conditions. H_3O^+ PBr_3 Mg, ether NaOH/H_2O, heat PCC Br_2 NaOH, H_2O LiAlH_4
Starting with benzene and any reagents you need, synthesize compound shown. More than one step is...
Starting with benzene and any reagents you need, synthesize compound shown. More than one step is required. Assume you can separate ortho and para-isomers. (12 pts) _CH₂
From the table of reagents shown below, show how you synthesize the product from the given...
From the table of reagents shown below, show how you synthesize the product from the given reactant. Reagents available (Enter the letter(s) of the reagent(s) needed in the box, in the order that they must be used. No more than two steps are required to perform the synthesis. Note that a retrosynthetic arrow is used, and therefore the reactant is shown on the right.) Answer:
Devise a synthesis of (Z)-4,4-dimethyl-2-pentene using one of the starting materials and any of the reagents...
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 HCBCH HC=C–CH, HC=C=CH-CH, HC=C=CH-CH-CH-CH, остаток сн. HC=C–C–CH, Η. сн. HC=C–C–CH, CH, . Reagents a NaNH, NHI) diodoethane g 1-bromo-3-methylbutane į Hy / Lindlar catalyst b NaOH ІН,0 e 1-bromopropane ht-butyl bromide k H, NH (1) c iodomethane f...
4. Propose a synthesis to create 3,4-dimethyl-3-hexanol from 1-butene. You only need to show individual steps an...
4. Propose a synthesis to create 3,4-dimethyl-3-hexanol from 1-butene. You only need to show individual steps and reagents, you do not need to show mechanisms. You must use 1-butene as your ONLY source of carbon atoms. The convergent processes have been outlined for you. for STEP 1: Show how to synthesize butyl magnesium bromide from 1-butene (5 points): BrMg STEP 2: Show how to synthesize 2-butanone from 1-butene (5 points): STEP 3: What intermediate forms below and what reagent(s) will...
References Devise a synthesis of (Z) 4-nonene using one of the starting materials and any of...
References Devise a synthesis of (Z) 4-nonene 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 CHO HC C-CCH CH HC CH HCЕC-CH, нC-C-сH,сн, HC-C-сH,сH,сH,сн, HCEC-CH H сн, 6 1 2 3 5 Reagents a NaNH, / NH,) g1-bromo-3-methy butane d iodoethane J H2/Lindlar cataly st b NaOH/H20 e 1-bromopropane k HINH,0)...
You need synthesize cyclopentanone starting with the lactone shown below in 9 steps where 3 of the steps are acid workups. A LDA B LAH C heat D H30 (aqueous acid) E PCC F NaOH, heat G NaOCH2CH Na Cr207, aq acid H HOCH2CH, acid, heat NBS Note there are 3 reagents on this table that are not used ALL OTHERS ARE USEI
the steps are B,D,H,I,G,D,F,D,C
Synthesis You need synthesize cyclopentanone starting with the lactone shown below in 9 steps where 3 of the steps are acid workups. Cheat DH,O (aqueous acid) E pcc F NaOH, heat G NaOCHCH H Na,Cr,0,.aq acid HOCH,CH,, acid, heat NBS Note- there are 3 reagents on this table that are not used - ALL OTHERS ARE USEI Steps Reaction names Give the name of the type of reaction for each step, (examples: acidification, reduction, saponification decarboxylation,...
Devise a synthesis of (Z)-3-octene 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 нсисынсно-си нос-сцен нос-cң соң,он нонс Reagents + NaNH / NH diodo ethane 1-bromo-3-methybutane H undar catalyst + NaOH HẠO e 1-bromopropane butyl bromide күн clodomethane 1 2-bromopropane H/Pd on carbon I N/NH0 Starting material Reagent for step 1...
The
reagent options are the same for all boxes
Trans-4-hexen-3-ol can be synthesized starting from acetaldehyde. One of the key reagents is ethyl grignard. Synthesize ethyl grignard from acetaldehyde in the steps below using the reagents provided. Synthesize (trans)-4-hexen-3-ol from acetaldehyde. Select the best reagents and conditions. H_3O^+ PBr_3 Mg, ether NaOH/H_2O, heat PCC Br_2 NaOH, H_2O LiAlH_4
Starting with benzene and any reagents you need, synthesize compound shown. More than one step is required. Assume you can separate ortho and para-isomers. (12 pts) _CH₂
From the table of reagents shown below, show how you synthesize the product from the given reactant. Reagents available (Enter the letter(s) of the reagent(s) needed in the box, in the order that they must be used. No more than two steps are required to perform the synthesis. Note that a retrosynthetic arrow is used, and therefore the reactant is shown on the right.) Answer:
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 HCBCH HC=C–CH, HC=C=CH-CH, HC=C=CH-CH-CH-CH, остаток сн. HC=C–C–CH, Η. сн. HC=C–C–CH, CH, . Reagents a NaNH, NHI) diodoethane g 1-bromo-3-methylbutane į Hy / Lindlar catalyst b NaOH ІН,0 e 1-bromopropane ht-butyl bromide k H, NH (1) c iodomethane f...
4. Propose a synthesis to create 3,4-dimethyl-3-hexanol from 1-butene. You only need to show individual steps and reagents, you do not need to show mechanisms. You must use 1-butene as your ONLY source of carbon atoms. The convergent processes have been outlined for you. for STEP 1: Show how to synthesize butyl magnesium bromide from 1-butene (5 points): BrMg STEP 2: Show how to synthesize 2-butanone from 1-butene (5 points): STEP 3: What intermediate forms below and what reagent(s) will...
References Devise a synthesis of (Z) 4-nonene 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 CHO HC C-CCH CH HC CH HCЕC-CH, нC-C-сH,сн, HC-C-сH,сH,сH,сн, HCEC-CH H сн, 6 1 2 3 5 Reagents a NaNH, / NH,) g1-bromo-3-methy butane d iodoethane J H2/Lindlar cataly st b NaOH/H20 e 1-bromopropane k HINH,0)...
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