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Hydrolysis of 2-bromo-2-methylpropane (tert-butyl...
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...
First step correct rest wrong---- Please provide clear drawing with arrows when necessary Hydrolysis of 2-bromo-2-methylpropane...
First step correct rest
wrong---- Please provide clear drawing with arrows when
necessary
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH3)3 CBr + 2H2O rightarrow (CH3)3 COH + H30+ + 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...
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH),CBr + 24,0 → (CH),COH + H20* + Br...
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH),CBr + 24,0 → (CH),COH + H20* + Br Give the Sn1 mechanism. Draw structures - including electrons and charges - and add curved arrows. Details count. Step 1 - Draw 2-bromo-2-methylpropane - Add one curved arrow. Draw the step 1 products: 1 organic species; 1 inorganic species. Map Step 2 . Reproduce the organic product of step 1. - Add one curved arrow to show water reacting with the organic species. Draw...
i am not sure what i am doing wrong for steps 2 3 and 4 of...
i am not sure what i am doing wrong for steps 2 3 and 4 of the
mechanism. can you draw them all out please and be specific as to
what exactly is shifting and to where.
Practice Problem 07.70b Draw the mechanism for the following reaction: conc. H,SO Heat (c) "OH Practice Problem 07.70b1 Correct. Add curved arrow(s) to draw step 1 of the mechanism. Modify the given drawing of the product as needed CH3 -CH3 CH, CH3 Edit...
RE klon 1 1 pt CH3 CH3 H₂O - H30* + cm ution 2 stion 3 stion 4 pt 18 1 pt H3C-¢-CI CH3 H3C---OH CH3 estion 5 1 pt 2...
RE klon 1 1 pt CH3 CH3 H₂O - H30* + cm ution 2 stion 3 stion 4 pt 18 1 pt H3C-¢-CI CH3 H3C---OH CH3 estion 5 1 pt 2-chloro-2-methylpropane reacts with water in three steps to yield 2-methylpropan-2-ol. One of these steps is shown below, add curved arrows to the mechanism to indicate the movement of electrons in this step. estion 6 1pt Arrow-pushing Instructions Question 7 1 pt Question 8 Question Question 10 1 pt pt pe...
For the following reaction: 1) Add curved arrows for the first step. 2) Draw both the...
For the following reaction: 1) Add curved arrows for the first step. 2) Draw both the organic and inorganic intermediate species. Include nonbonding electrons and charges, where applicable. Include hydrogen atoms. CH3 H3C CH3 H₃ C & &-CH₃
Show the curved arrow mechanism for the reaction...
1.2.3.4.5.6.7.8.Show the curved arrow mechanism for the reaction between ethoxide and methanol to give ethanol and the methoxide ion. 1st attempt Jual See Periodic Table See Hint OH-Ö: Add the missing curved arrow notation.The carbon-metal bond in organometallic Grignard reagents exhibits significant covalent character. However, we can treat these compounds as electron-rich carbanions because of the large difference in electronegativity between carbon and magnesium. These reagents are great to form carbon-carbon bonds but must be kept in an anhydrous environment...
Part 1 involved MeOH addition to form the key tetrahedral intermediate. Part 2 involves loss of H2O from the Map t...
Part 1 involved MeOH addition to form the key tetrahedral intermediate. Part 2 involves loss of H2O from the Map tetrahedral intermediate to form the ester. Part 2 of 2 Intermediate species (from Part 1); Add two curved arrows for the next step. Hö: CH3 er all remaining steps in the mechanism: 1) Draw each species (organic and inorganic) resulting from the previous step. Each step will include all of, and only, the atoms given in the first step i.e.,...
The Claisen condensation converts 2 molecules of an ester into a B-keto ester. The reaction starts...
The Claisen condensation converts 2 molecules of an ester into a B-keto ester. The reaction starts with the ester in an alkoxide/alcohol solution and is worked up with acid to form the neutral B-keto ester product. :0 O: 1. -OCH2CH3/CH3CH20H 2 2. H30 OH Show the curved-arrow mechanism for the Claisen condensation of ethyl ethanoate treated with ethoxide ion. Include all formal charges and nonbonding electrons. In each step, draw only the species that react in that step. If an...
1-24 need help really lost Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for...
1-24 need help really lost
Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for the following deprotonation step. Also add the other product notice how the Tema s can be converted to this by use of a strong base such as sodium a sodium ion (Na) is not drawn, in this case it is just a spectatorio PCW27 - Mechanistic steps - Part Name: Time spent 2) Label the above compounds with the appropriate name from the previous...
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...
First step correct rest
wrong---- Please provide clear drawing with arrows when
necessary
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH3)3 CBr + 2H2O rightarrow (CH3)3 COH + H30+ + 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...
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH),CBr + 24,0 → (CH),COH + H20* + Br Give the Sn1 mechanism. Draw structures - including electrons and charges - and add curved arrows. Details count. Step 1 - Draw 2-bromo-2-methylpropane - Add one curved arrow. Draw the step 1 products: 1 organic species; 1 inorganic species. Map Step 2 . Reproduce the organic product of step 1. - Add one curved arrow to show water reacting with the organic species. Draw...
i am not sure what i am doing wrong for steps 2 3 and 4 of the
mechanism. can you draw them all out please and be specific as to
what exactly is shifting and to where.
Practice Problem 07.70b Draw the mechanism for the following reaction: conc. H,SO Heat (c) "OH Practice Problem 07.70b1 Correct. Add curved arrow(s) to draw step 1 of the mechanism. Modify the given drawing of the product as needed CH3 -CH3 CH, CH3 Edit...
RE klon 1 1 pt CH3 CH3 H₂O - H30* + cm ution 2 stion 3 stion 4 pt 18 1 pt H3C-¢-CI CH3 H3C---OH CH3 estion 5 1 pt 2-chloro-2-methylpropane reacts with water in three steps to yield 2-methylpropan-2-ol. One of these steps is shown below, add curved arrows to the mechanism to indicate the movement of electrons in this step. estion 6 1pt Arrow-pushing Instructions Question 7 1 pt Question 8 Question Question 10 1 pt pt pe...
For the following reaction: 1) Add curved arrows for the first step. 2) Draw both the organic and inorganic intermediate species. Include nonbonding electrons and charges, where applicable. Include hydrogen atoms. CH3 H3C CH3 H₃ C & &-CH₃
1.2.3.4.5.6.7.8.Show the curved arrow mechanism for the reaction between ethoxide and methanol to give ethanol and the methoxide ion. 1st attempt Jual See Periodic Table See Hint OH-Ö: Add the missing curved arrow notation.The carbon-metal bond in organometallic Grignard reagents exhibits significant covalent character. However, we can treat these compounds as electron-rich carbanions because of the large difference in electronegativity between carbon and magnesium. These reagents are great to form carbon-carbon bonds but must be kept in an anhydrous environment...
Part 1 involved MeOH addition to form the key tetrahedral intermediate. Part 2 involves loss of H2O from the Map tetrahedral intermediate to form the ester. Part 2 of 2 Intermediate species (from Part 1); Add two curved arrows for the next step. Hö: CH3 er all remaining steps in the mechanism: 1) Draw each species (organic and inorganic) resulting from the previous step. Each step will include all of, and only, the atoms given in the first step i.e.,...
The Claisen condensation converts 2 molecules of an ester into a B-keto ester. The reaction starts with the ester in an alkoxide/alcohol solution and is worked up with acid to form the neutral B-keto ester product. :0 O: 1. -OCH2CH3/CH3CH20H 2 2. H30 OH Show the curved-arrow mechanism for the Claisen condensation of ethyl ethanoate treated with ethoxide ion. Include all formal charges and nonbonding electrons. In each step, draw only the species that react in that step. If an...
1-24 need help really lost
Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for the following deprotonation step. Also add the other product notice how the Tema s can be converted to this by use of a strong base such as sodium a sodium ion (Na) is not drawn, in this case it is just a spectatorio PCW27 - Mechanistic steps - Part Name: Time spent 2) Label the above compounds with the appropriate name from the previous...
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