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(a) Draw the neutral organic product when butanone reacts with 1 equivalent of ethanol in acidic...
(a) Draw the neutral organic product when butanone reacts with 1 equivalent of ethanol in acidic...
(a) Draw the neutral organic product when butanone reacts with 1 equivalent of ethanol in acidic solution. HCI +CH,CH.OH (b) Below, write a curved-arrow mechanism for this reaction. Each answer field should be treated as a closed system (.e, atom conservation). Details count Step 1. The reactants are given; add the appropriate curved arrows) ト-Cl:
(a) Draw the neutral organic product when butanone reacts with 1 equivalent of ethanol in acidic...
(a) Draw the neutral organic product when butanone reacts with 1 equivalent of ethanol in acidic solution Show all lone pairs and non-zero formal charges HO + CH,CH,OH → (by Below, write a curved-arrow mechanism for this reaction. Each answer field should be treated as a dosed system (ie, atom conservation) Details count! Step 1. The reactants are given, add the appropriate curved arrow(). View Che Answer Net hout e n privacy policy terms of use contact DOLL Gradebook 11/4/2019...
draw the neutral organic product when butanone reacts with 1 equivalent of ethanol in acidic solution.
draw the neutral organic product when butanone reacts with 1
equivalent of ethanol in acidic solution.
please answer and label all steps Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (сн), сон +...
please answer and label all steps
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (сн), сон + н,о* + CH CBr 2H,O Br Give the SN1 mechanism. The reactants are already given in step 1; you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count Note: You should have 4 carbon atoms, 13...
everything is correct except for step 3 i dont know whats wrong Hydrolysis of 2-bromo-2-methylpropane (tert-butyl...
everything is correct except for step 3 i dont know whats
wrong
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH),CBr + 2H,0 → (CH),COH + H,0* + Br Give the Sn1 mechanism. The reactants are already given in step 1: you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count. Note: You...
7. Shown below are the major product formed and the proposed mechanism when 1- methylcyclohexanol reacts...
7. Shown below are the major product formed and the proposed mechanism when 1- methylcyclohexanol reacts with 85% H3PO4 at 150 °C. Name all curved arrows shown in each step as either "lone pair to bond" or "bond to long pair". Specify the atom that donates/accepts the lone pair. [1 Mark] Step 1 -H O ro-H + Ho + H2O H H Commons Kagamo Step 2 + H2O Step 3 = + H,PO. H HAPO Zaitsev product 6. Given below...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyri...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
1. 2. JUST DRAW ARROWS... (CH3)2Culi + CH3Cu Ph CI Ph CH3 The ketone intermediate formed...
1.
2.
JUST DRAW ARROWS...
(CH3)2Culi + CH3Cu Ph CI Ph CH3 The ketone intermediate formed in the reaction of an acid chloride with a Grignard reagent cannot be isolated because it reacts too rapidly with the second equivalent of Grignard reagent. To produce a ketone from an acid chloride, one can treat the acid chloride with a lithium dialkylcopper reagent. The reaction occurs by nucleophilic acyl substitution on the acid chloride by the dialkylcopper anion to yield an acyl...
1 pt 1 pt The final step in the hydration of an alkyne under acidic conditions...
1 pt 1 pt The final step in the hydration of an alkyne under acidic conditions is the automerization of an enol intermediate to give the corresponding ketone. The mechanism involves a protonation followed by deprotonation Consider the following tautomerization reaction: CH2 CHE H,09 1 pt 1 pt 1 pt OH 1 pt 1pl For the mechanism step below, draw curved arrows to show electron reorganization Where relevant, a pi bond has two hot spots when you draw a curved...
Please answer al three questions. Thank you!! I Review I Constants I Periodic Table When a...
Please answer al three questions. Thank you!!
I Review I Constants I Periodic Table When a chemical reaction occurs, atoms rearrange to form new compounds, but no new atoms are created nor are any destroyed. This concept is called conservation of Part A mass. Mass conservation can be seen in a balanced chemical equation, where the numbers of each kind of atom are the same on both sides of the reaction arrow. The figure (Figure 1) shows the reaction of...
(a) Draw the neutral organic product when butanone reacts with 1 equivalent of ethanol in acidic solution. HCI +CH,CH.OH (b) Below, write a curved-arrow mechanism for this reaction. Each answer field should be treated as a closed system (.e, atom conservation). Details count Step 1. The reactants are given; add the appropriate curved arrows) ト-Cl:
(a) Draw the neutral organic product when butanone reacts with 1 equivalent of ethanol in acidic solution Show all lone pairs and non-zero formal charges HO + CH,CH,OH → (by Below, write a curved-arrow mechanism for this reaction. Each answer field should be treated as a dosed system (ie, atom conservation) Details count! Step 1. The reactants are given, add the appropriate curved arrow(). View Che Answer Net hout e n privacy policy terms of use contact DOLL Gradebook 11/4/2019...
draw the neutral organic product when butanone reacts with 1
equivalent of ethanol in acidic solution.
please answer and label all steps
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (сн), сон + н,о* + CH CBr 2H,O Br Give the SN1 mechanism. The reactants are already given in step 1; you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count Note: You should have 4 carbon atoms, 13...
everything is correct except for step 3 i dont know whats
wrong
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH),CBr + 2H,0 → (CH),COH + H,0* + Br Give the Sn1 mechanism. The reactants are already given in step 1: you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count. Note: You...
7. Shown below are the major product formed and the proposed mechanism when 1- methylcyclohexanol reacts with 85% H3PO4 at 150 °C. Name all curved arrows shown in each step as either "lone pair to bond" or "bond to long pair". Specify the atom that donates/accepts the lone pair. [1 Mark] Step 1 -H O ro-H + Ho + H2O H H Commons Kagamo Step 2 + H2O Step 3 = + H,PO. H HAPO Zaitsev product 6. Given below...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
1.
2.
JUST DRAW ARROWS...
(CH3)2Culi + CH3Cu Ph CI Ph CH3 The ketone intermediate formed in the reaction of an acid chloride with a Grignard reagent cannot be isolated because it reacts too rapidly with the second equivalent of Grignard reagent. To produce a ketone from an acid chloride, one can treat the acid chloride with a lithium dialkylcopper reagent. The reaction occurs by nucleophilic acyl substitution on the acid chloride by the dialkylcopper anion to yield an acyl...
1 pt 1 pt The final step in the hydration of an alkyne under acidic conditions is the automerization of an enol intermediate to give the corresponding ketone. The mechanism involves a protonation followed by deprotonation Consider the following tautomerization reaction: CH2 CHE H,09 1 pt 1 pt 1 pt OH 1 pt 1pl For the mechanism step below, draw curved arrows to show electron reorganization Where relevant, a pi bond has two hot spots when you draw a curved...
Please answer al three questions. Thank you!!
I Review I Constants I Periodic Table When a chemical reaction occurs, atoms rearrange to form new compounds, but no new atoms are created nor are any destroyed. This concept is called conservation of Part A mass. Mass conservation can be seen in a balanced chemical equation, where the numbers of each kind of atom are the same on both sides of the reaction arrow. The figure (Figure 1) shows the reaction of...
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