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9- Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary ad...
Show how you would synthesize the following a n d beginning with 1-butene, Bromma and any...
Show how you would synthesize the following a n d beginning with 1-butene, Bromma and any necessary additional reagents. More than one step is needed. Br Bromobenzene, 1-Butene < Show how you woull Synthesize 4.- Nonanone, begining with 1-Butanol and any other non-organic reagents. (1-Butanol is the only Organic compouno available). only organ n
1. Which Wittig reagent would be used to synthesize 2 CH-CH=P(CAH) CH=P(CHẠh. P(CH3)3 CH,CH,CH-P(CH3)3 IV 2....
1. Which Wittig reagent would be used to synthesize 2 CH-CH=P(CAH) CH=P(CHẠh. P(CH3)3 CH,CH,CH-P(CH3)3 IV 2. What is the correct IUPAC name for the following compound? 6 eye 3. What is the correct structure for 7-methyl-4-octanone? 3 4. The products, D and E, of the following reaction sequence, S "CN HCI HCN CH.NO H20 heat would be: CH2CH2CN CH,CH,MgBe HO E ? ether Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary additional reagents....
Show how you would synthesize the following compound starting with acetylene and compounds containing no more...
Show how you would synthesize the following compound starting
with acetylene and compounds containing no more than two carbon
atoms as organic starting material. You may use any additional
reagents you need
Br H H Br
4. In each reaction show how you would synthesize the product from the reactant. Show the...
4. In each reaction show how you would synthesize the product
from the reactant. Show the reagents, conditions, and the
structures of any important intermediates along the way. Any
organic reagent may be used, and more than one step may be used as
well. Include mechanism
(+-) H Br
Show how the following compound could be prepared from 1-butyne. You may use any necessary reagents....
Show how the following compound could be prepared from 1-butyne. You may use any necessary reagents. You must show all stable intermediates formed along the way and all necessary reagents used (20 points). multiple steps! Br
Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting...
Show how you would use Grignard syntheses to prepare the
following alcohols from the indicated starting materials and any
other necessary reagents. Draw the Grignard reagent and any other
organic reagents needed.
11 RUVIUWI Constans i Pendulu Part F Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting materials and any other necessary reagents. Draw the Grignard reagent and any other organic reagents needed. ОН -C-CH CH, from C-OCH.CH Draw the molecules on...
1. 2. Show how you would synthesize benzylamine from each of these compounds, using the following...
1.
2.
Show how you would synthesize benzylamine from each of these compounds, using the following available reagents More than one step may be required. Enter the letters of the reagents necessary, in the order that they are to be used. Do not separate the reagents with punctuation. OH CI Reagents Available (a) NH3 (b) excess NH3 (c) H*, A (d) SOCl2 (e) N3 (f) H2, Pd/C (g) LiAlH4 then H20 (h) NaOH (i) CO, H2, heat and pressure Previous...
organic chemistry 1.1 pt) Which reagent would you use to effect the following transformation of a...
organic chemistry
1.1 pt) Which reagent would you use to effect the following transformation of a diol into a keto acid? ОН Reagent? CH,CHCH,CH,CH,OH - CH,CCH,CH,сон a) Jones(H2Cr2O7) b) Tollens c) mCPBA d) Collins(PCC) e) LiAlH4 2.(2 pts) Circle the TWO compounds that yield a stable Grignard reagent when treated with magnesium in ether. Br CHÚC HỌC=CH- CH,OH HN 3.(2 pts each) Reactions. Complete each reaction shown here. HỌC=CH- + HC=CH- -CH OH он 1. CH CH MgBrCH,CH,CH=CHCCH2CH3 2.H2O Сн,...
Select the reagents you would use to synthesize the compound below from benzene. (More than one...
Select the reagents you would use to synthesize the compound
below from benzene.
(More than one step is required. If no third step is needed,
choose (none).)
Reagents Available f. KMnO4, H20 g. H2, Pd/C h. SO3, H2SO4 i. NaOH, H2O a. Br2, FeBr3 b. Cl2, FeCl 0 d. CH3CI, AICl3 Br e. CH3COCI, AICl3 N-bromosuccinimide (NBS) ball & stick labels Step 1: Step 2 Step 3
? How would you carry out the following conversion? Show only the reagents needed for each...
?
How would you carry out the following conversion? Show only the reagents needed for each step and the structure of any intermediate formed with appropriate stereochemistry if necessary. More than one step may be necessary. No need to provide mechanisms but make sure you clearly indicate all reagents and intermediates. etb eo h flowing cosvesian? [10 marks] OH HO HO
Show how you would synthesize the following a n d beginning with 1-butene, Bromma and any necessary additional reagents. More than one step is needed. Br Bromobenzene, 1-Butene < Show how you woull Synthesize 4.- Nonanone, begining with 1-Butanol and any other non-organic reagents. (1-Butanol is the only Organic compouno available). only organ n
1. Which Wittig reagent would be used to synthesize 2 CH-CH=P(CAH) CH=P(CHẠh. P(CH3)3 CH,CH,CH-P(CH3)3 IV 2. What is the correct IUPAC name for the following compound? 6 eye 3. What is the correct structure for 7-methyl-4-octanone? 3 4. The products, D and E, of the following reaction sequence, S "CN HCI HCN CH.NO H20 heat would be: CH2CH2CN CH,CH,MgBe HO E ? ether Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary additional reagents....
Show how you would synthesize the following compound starting
with acetylene and compounds containing no more than two carbon
atoms as organic starting material. You may use any additional
reagents you need
Br H H Br
4. In each reaction show how you would synthesize the product
from the reactant. Show the reagents, conditions, and the
structures of any important intermediates along the way. Any
organic reagent may be used, and more than one step may be used as
well. Include mechanism
(+-) H Br
Show how the following compound could be prepared from 1-butyne. You may use any necessary reagents. You must show all stable intermediates formed along the way and all necessary reagents used (20 points). multiple steps! Br
Show how you would use Grignard syntheses to prepare the
following alcohols from the indicated starting materials and any
other necessary reagents. Draw the Grignard reagent and any other
organic reagents needed.
11 RUVIUWI Constans i Pendulu Part F Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting materials and any other necessary reagents. Draw the Grignard reagent and any other organic reagents needed. ОН -C-CH CH, from C-OCH.CH Draw the molecules on...
1.
2.
Show how you would synthesize benzylamine from each of these compounds, using the following available reagents More than one step may be required. Enter the letters of the reagents necessary, in the order that they are to be used. Do not separate the reagents with punctuation. OH CI Reagents Available (a) NH3 (b) excess NH3 (c) H*, A (d) SOCl2 (e) N3 (f) H2, Pd/C (g) LiAlH4 then H20 (h) NaOH (i) CO, H2, heat and pressure Previous...
organic chemistry
1.1 pt) Which reagent would you use to effect the following transformation of a diol into a keto acid? ОН Reagent? CH,CHCH,CH,CH,OH - CH,CCH,CH,сон a) Jones(H2Cr2O7) b) Tollens c) mCPBA d) Collins(PCC) e) LiAlH4 2.(2 pts) Circle the TWO compounds that yield a stable Grignard reagent when treated with magnesium in ether. Br CHÚC HỌC=CH- CH,OH HN 3.(2 pts each) Reactions. Complete each reaction shown here. HỌC=CH- + HC=CH- -CH OH он 1. CH CH MgBrCH,CH,CH=CHCCH2CH3 2.H2O Сн,...
Select the reagents you would use to synthesize the compound
below from benzene.
(More than one step is required. If no third step is needed,
choose (none).)
Reagents Available f. KMnO4, H20 g. H2, Pd/C h. SO3, H2SO4 i. NaOH, H2O a. Br2, FeBr3 b. Cl2, FeCl 0 d. CH3CI, AICl3 Br e. CH3COCI, AICl3 N-bromosuccinimide (NBS) ball & stick labels Step 1: Step 2 Step 3
?
How would you carry out the following conversion? Show only the reagents needed for each step and the structure of any intermediate formed with appropriate stereochemistry if necessary. More than one step may be necessary. No need to provide mechanisms but make sure you clearly indicate all reagents and intermediates. etb eo h flowing cosvesian? [10 marks] OH HO HO
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