Homework Answers
Answer is c).
In dehydration reaction, both OH and H must be at antiperiplanar to each other and only then dehydration takes place.
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Dehydration WILL NOT produce the desired product from the given starting material. (See questions 20-23 for...
QUESTION 20 Consider the dehydration reaction using the starting material shown below to answer questions 20-23...
QUESTION 20 Consider the dehydration reaction using the starting material shown below to answer questions 20-23 Dehydration Which reagent(s) are required to perform a dehydration reaction? o a. HCI С. NaH o d. H2SO4 e. NaOH f, H2SO4, heat g. NaOH, heat QUESTION 21 Identify all carbocations that appear in the mechansim for this reaction. Choose all that apply iv) a. C. eNone of the above. The reaction goes by an E2 mechanism and no carbocations are formed. QUESTION 22...
Consider the dehydration reaction using the starting material shown below to answer questions 20-23. НО Dehydration...
Consider the dehydration reaction using the starting material shown below to answer questions 20-23. НО Dehydration Identify all carbocations that appear in the mechansim for this reaction. Choose all that apply. iv) ii) a. i b. d. iv e. None of the above. The reaction goes by an E2 mechanism and no carbocations are formed.
For the reaction below, focus only on 2-methyl-2-butanol (starting material) and 2-chloro-2-methylbutane (desired product). We will...
For the reaction below, focus only on 2-methyl-2-butanol
(starting material) and 2-chloro-2-methylbutane (desired product).
We will not analyze HCl or H2O by IR.
From the two IR spectra below, identify which spectrum belongs
to which molecule. Then label the IR spectrum with the molecule’s
characteristic IR peaks. Highlight or place a box around the most
characteristic peak in the starting material’s IR. You do not need
to label the fingerprint region.
For the reaction below, focus only on 2-methyl-2-butanol...
need help with 1-21 1) Label the steps below as "slow" and "fast". HCH 013 10...
need help with 1-21
1) Label the steps below as "slow" and "fast". HCH 013 10 = H. C + + H-LG H-LG 2) Why are they slow/fast? Explain using chemical terms. Stereochemistry of the Sn1 reaction 3) What type of intermediate does the Sn1 reaction proceed through? 4) What is the geometry of the carbon that the nucleophile coordinates to in the 2 step? 5) From how many directions would it be reasonable for the nucleophile to approach the...
need help with the boxed bullet point. writing the chemical reaction scheme for the experiment. Synthesis of an A...
need help with the boxed bullet point. writing the chemical
reaction scheme for the experiment.
Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...
Product was formed successfully based on the exp. below (about 85% yield), please interpret/discuss HNMR/IR in...
Product was formed successfully based on the exp. below (about
85% yield), please interpret/discuss HNMR/IR in as much detail as
possible and assign peaks on HNMR (which peak represents which
protons of which group, etc). Note: I already know how you
determine the formation of the product so you can skip that part of
part b).
Based on this exp:
Discuss the IR spectrum and what is the peak in IR that you can see for a specific functional group...
Can you help me identify reagent (i), Compound 8 and Compound 12 in the reaction scheme?...
Can you help me identify reagent (i), Compound 8 and
Compound 12 in the reaction scheme?
You have laboratory data on all the compounds in the
synthesis, however the amount of data available to you varies. Some
have the entirety of the spectral data, others have as little as
the elemental analysis. Use the laboratory data to help you
discover which reaction has been performed.
The lab data for Compound 8 and 12 is as
follows:
You can use any...
Working on the questions at the end of this lab report (see above). I need help answering questio...
Working on the questions at the end of this lab report
(see above). I need help answering questions 2, 3, and 4 completely
and thoroughly. Thank you!
s, until the I hexano 1 clean disti CYCLOHEXENE from CYCLOHEXANOL be dehydrated with solfuric acid to yield cyclohexene and waterf Add a 0°C (record ct and cal H,SO + H20 ainer. s in purification of any crude product are (a) the preliminary separation of the product from the reaction mixture by distillation...
help please? this was the only other information given REPORT SHEET Determination of the Solubility-Product Constant...
help please?
this was the only other information given
REPORT SHEET Determination of the Solubility-Product Constant for a Sparingly Soluble Salt EXPERIMENT 8 A. Preparation of a Calibration Curve Initial (Cro121 0.0024 M Absorbance 5 mL Volume of 0.0024 M K Cro Total volume 1. I mL 100 mL 2. 100ML 3. 10 mL 100ml 4. 15 mL 100 ML Molar extinction coefficient for [CrO2) [Cro,2) 2.4x100M 12x1044 2.4810M 3.6810M 0.04) 2037.37 0.85 1.13 2. 3. Average molar extinction coefficient...
5. When all of the sample to be collected has left the column, will the drop...
5. When all of the sample to be collected has left the
column, will the drop of solution coming off the tip of the column
be acidic, basic or neutral?
6. How many H+ ions would be displaced from the ion
exchange column by 1 Cu2+ ion?
7. Binding sites on the ion exchange resin are saturated
with which ion before the sample solution is added?
8. Ions are displaced from the resin binding sites by
any ion that has...
QUESTION 20 Consider the dehydration reaction using the starting material shown below to answer questions 20-23 Dehydration Which reagent(s) are required to perform a dehydration reaction? o a. HCI С. NaH o d. H2SO4 e. NaOH f, H2SO4, heat g. NaOH, heat QUESTION 21 Identify all carbocations that appear in the mechansim for this reaction. Choose all that apply iv) a. C. eNone of the above. The reaction goes by an E2 mechanism and no carbocations are formed. QUESTION 22...
Consider the dehydration reaction using the starting material shown below to answer questions 20-23. НО Dehydration Identify all carbocations that appear in the mechansim for this reaction. Choose all that apply. iv) ii) a. i b. d. iv e. None of the above. The reaction goes by an E2 mechanism and no carbocations are formed.
For the reaction below, focus only on 2-methyl-2-butanol
(starting material) and 2-chloro-2-methylbutane (desired product).
We will not analyze HCl or H2O by IR.
From the two IR spectra below, identify which spectrum belongs
to which molecule. Then label the IR spectrum with the molecule’s
characteristic IR peaks. Highlight or place a box around the most
characteristic peak in the starting material’s IR. You do not need
to label the fingerprint region.
For the reaction below, focus only on 2-methyl-2-butanol...
need help with 1-21
1) Label the steps below as "slow" and "fast". HCH 013 10 = H. C + + H-LG H-LG 2) Why are they slow/fast? Explain using chemical terms. Stereochemistry of the Sn1 reaction 3) What type of intermediate does the Sn1 reaction proceed through? 4) What is the geometry of the carbon that the nucleophile coordinates to in the 2 step? 5) From how many directions would it be reasonable for the nucleophile to approach the...
need help with the boxed bullet point. writing the chemical
reaction scheme for the experiment.
Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...
Product was formed successfully based on the exp. below (about
85% yield), please interpret/discuss HNMR/IR in as much detail as
possible and assign peaks on HNMR (which peak represents which
protons of which group, etc). Note: I already know how you
determine the formation of the product so you can skip that part of
part b).
Based on this exp:
Discuss the IR spectrum and what is the peak in IR that you can see for a specific functional group...
Can you help me identify reagent (i), Compound 8 and
Compound 12 in the reaction scheme?
You have laboratory data on all the compounds in the
synthesis, however the amount of data available to you varies. Some
have the entirety of the spectral data, others have as little as
the elemental analysis. Use the laboratory data to help you
discover which reaction has been performed.
The lab data for Compound 8 and 12 is as
follows:
You can use any...
Working on the questions at the end of this lab report
(see above). I need help answering questions 2, 3, and 4 completely
and thoroughly. Thank you!
s, until the I hexano 1 clean disti CYCLOHEXENE from CYCLOHEXANOL be dehydrated with solfuric acid to yield cyclohexene and waterf Add a 0°C (record ct and cal H,SO + H20 ainer. s in purification of any crude product are (a) the preliminary separation of the product from the reaction mixture by distillation...
help please?
this was the only other information given
REPORT SHEET Determination of the Solubility-Product Constant for a Sparingly Soluble Salt EXPERIMENT 8 A. Preparation of a Calibration Curve Initial (Cro121 0.0024 M Absorbance 5 mL Volume of 0.0024 M K Cro Total volume 1. I mL 100 mL 2. 100ML 3. 10 mL 100ml 4. 15 mL 100 ML Molar extinction coefficient for [CrO2) [Cro,2) 2.4x100M 12x1044 2.4810M 3.6810M 0.04) 2037.37 0.85 1.13 2. 3. Average molar extinction coefficient...
5. When all of the sample to be collected has left the
column, will the drop of solution coming off the tip of the column
be acidic, basic or neutral?
6. How many H+ ions would be displaced from the ion
exchange column by 1 Cu2+ ion?
7. Binding sites on the ion exchange resin are saturated
with which ion before the sample solution is added?
8. Ions are displaced from the resin binding sites by
any ion that has...
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