Please help with this question. My last name starts with K so these are the conditions I was give...
Please help with this question. My last name starts with K so these are the conditions I was given.
You will propose three synthetic schemes that will have as final product a secondary alcohol starting from an alkene with the following conditions:
Z alkene, acyclic (no rings) if your last name starts with I-P (with no more than 7 carbon atoms and no less than 4 carbon atoms)
All the proposed schemes should have the intermediates and the final product as major components.
You will predict the 1H NMR spectra (chemical shift, multiplicity and integral) of the starting alkene and the final product, alcohol.
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Please help with this question. My last name starts with K so these are the conditions I was give...
please help The dehydration of alcohols Under acidic conditions, alcohols will undergo a dehydration reaction, producing...
please help
The dehydration of alcohols Under acidic conditions, alcohols will undergo a dehydration reaction, producing an alkene and water. During the reaction, the hydroxyl group of the alcohol and a hydrogen atom from an adjacent carbon atom are lost. The reaction takes place in three steps, as shown in the diagram. (Figure 1) In the first step, a hydrogen lon bonds to the hydroxyl group of the alcohol. In the second step, the protonated hydroxl group leaves the compound,...
Please help! i will give a thumbs up immediately! From any source you like, choose a...
Please help! i will give a thumbs up immediately! From any source you like, choose a natural product (an organic compound or substance produced by a living organism that is found in nature) with not more than 18 and not less than six carbon atoms. Draw the structure of your compound including stereochemical information, report a name, the molecular formula and molar mass. (5 pts.) Cite one publication that describes the synthesis of this molecule, check e. g. Google Scholar....
please please my last question, i will give 5 stars, thank u!!!! Warch of the following...
please please my last question, i will give 5 stars, thank
u!!!!
Warch of the following is the permeability of biological A. Cholesterol binds to the w ide varice of solutes. obiads to the outside worl B. Because choledere is which C. Because cholesterol is hihe diffusion through the membrane olesterol is a hydrocarbon that has twins in solutes from moving easily is w chehen th What is the name of the is the name of the currently do c...
Please help with the question that I have circled in red. This is from a lab...
Please help with the question that I have circled in red. This
is from a lab I did and I have included the entire handout in case
it helps you to answer the question.
2015 Chem 263 2-Credit Org Lab 6T: Dehydration of Cyclohexanol to Cyclohexene Lab 6T w lecture you recently learned that alkenes undergo acid-catalyzed addition of H20 (hydration of the alkene) to yield alcohols. This lab with illustrate the same chemistry in reverse; the microscopic reverse of...
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...
Chapter 11: 1. What is a prime rule in naming alkenes? a. Find the longest carbon...
Chapter 11: 1. What is a prime rule in naming alkenes? a. Find the longest carbon chain. b.Find the longest carbon chain containing the alkene. c. Find whether the alkene has a cis- or trans- configuration. d.Find how far the alkene functionality is from either end. 2. What is the IUPAC name of the following alkene? a. cis-5-methyl-2-heptene b. trans-2-ethyl-4-hexene c. trans-5-methyl-2-heptene d. trans-3-methyl-5-heptene 3. What is the hybridization, geometry, and bond angle of the carbon marked by an asterisk?...
please need help with all the questions and ASAP, thank you 11. Please predict the principle...
please need help with all the questions and ASAP, thank you
11. Please predict the principle organic product of the following reactions, show stereochemistry where appropriate. Note that some reactions involve isotope-labeled compounds, in those cases the correct isotope must be used. (66') 1. LIAID 2. H,O (1) 18 1) THF (2). CH3Li + 2) HaO NaBH4 (3) CH3OD H2(excess)/Pt (4) d herd (5). - Mg Br D2O diethyl ether Br +Li (6) diethyl ether LICu(CH2CHs)2 Br (7). 1. diethyl...
Hi i need to known unknown molecule, functional group, 1hnmr , 13cnmr information and please give...
Hi
i need to known unknown molecule, functional group, 1hnmr ,
13cnmr information and please give me information about ir spectra
using NMR data given.
Carhonyl carbons Aldehydes/Ketones Carboxylic acid derivatives (Acids, amides, esters) Pi-system carbons Aromatics Alkynes Alkenes Carbons with electronegative atoms or groups Ethers/Alcohols (X=0) lodides (X = 1) Other Groups (CI, Br, N. C=C, CHO) Alkyl carbons Methine Methylene Methyl 225 200 175 150 125 100 Chemical Shift (ppm) 75 25 Protons adjacent to electron withdrawing groups...
**(left structure)****(right structure)** The two structures for the assignment are above and the task is: 1....
**(left structure)****(right
structure)**
The two structures for the assignment are above and
the task is:
1. Perform a retrosynthetic analysis on the two target
molecules assigned to you. In each case the organic
starting material (what you have to work backwards toward) depends
upon the target. For the structure given above (structure on left),
the starting material is either malonic ester or acetoacetic ester
and any halide. For the structure given above (structure on right),
the starting material is any...
How to solve alkene and alkyne reactions - Merdanym i Act antalyzod Hrdian ca Come Lazarmistry...
How to solve alkene and alkyne reactions
- Merdanym i Act antalyzod Hrdian ca Come Lazarmistry I V WORKSHOP #9 Alkenes, Alkynes, Reactions 1. Give a reasonable mechanism for the following reaction. Clearly show intermediates and show the movement of electron pairs with curved arrows. all сна H20. (H2SO4) H₃C CH₂ нас он H3CX сна 2. The addition of HBr to 2-methylpropene can, in principle, give either 1-bromo-2- methylpropane or 2-bromo-2-methylpropane. In reality, only the latter is formed. Show mechanisms...
please help
The dehydration of alcohols Under acidic conditions, alcohols will undergo a dehydration reaction, producing an alkene and water. During the reaction, the hydroxyl group of the alcohol and a hydrogen atom from an adjacent carbon atom are lost. The reaction takes place in three steps, as shown in the diagram. (Figure 1) In the first step, a hydrogen lon bonds to the hydroxyl group of the alcohol. In the second step, the protonated hydroxl group leaves the compound,...
please please my last question, i will give 5 stars, thank
u!!!!
Warch of the following is the permeability of biological A. Cholesterol binds to the w ide varice of solutes. obiads to the outside worl B. Because choledere is which C. Because cholesterol is hihe diffusion through the membrane olesterol is a hydrocarbon that has twins in solutes from moving easily is w chehen th What is the name of the is the name of the currently do c...
Please help with the question that I have circled in red. This
is from a lab I did and I have included the entire handout in case
it helps you to answer the question.
2015 Chem 263 2-Credit Org Lab 6T: Dehydration of Cyclohexanol to Cyclohexene Lab 6T w lecture you recently learned that alkenes undergo acid-catalyzed addition of H20 (hydration of the alkene) to yield alcohols. This lab with illustrate the same chemistry in reverse; the microscopic reverse of...
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...
please need help with all the questions and ASAP, thank you
11. Please predict the principle organic product of the following reactions, show stereochemistry where appropriate. Note that some reactions involve isotope-labeled compounds, in those cases the correct isotope must be used. (66') 1. LIAID 2. H,O (1) 18 1) THF (2). CH3Li + 2) HaO NaBH4 (3) CH3OD H2(excess)/Pt (4) d herd (5). - Mg Br D2O diethyl ether Br +Li (6) diethyl ether LICu(CH2CHs)2 Br (7). 1. diethyl...
Hi
i need to known unknown molecule, functional group, 1hnmr ,
13cnmr information and please give me information about ir spectra
using NMR data given.
Carhonyl carbons Aldehydes/Ketones Carboxylic acid derivatives (Acids, amides, esters) Pi-system carbons Aromatics Alkynes Alkenes Carbons with electronegative atoms or groups Ethers/Alcohols (X=0) lodides (X = 1) Other Groups (CI, Br, N. C=C, CHO) Alkyl carbons Methine Methylene Methyl 225 200 175 150 125 100 Chemical Shift (ppm) 75 25 Protons adjacent to electron withdrawing groups...
**(left structure)****(right
structure)**
The two structures for the assignment are above and
the task is:
1. Perform a retrosynthetic analysis on the two target
molecules assigned to you. In each case the organic
starting material (what you have to work backwards toward) depends
upon the target. For the structure given above (structure on left),
the starting material is either malonic ester or acetoacetic ester
and any halide. For the structure given above (structure on right),
the starting material is any...
How to solve alkene and alkyne reactions
- Merdanym i Act antalyzod Hrdian ca Come Lazarmistry I V WORKSHOP #9 Alkenes, Alkynes, Reactions 1. Give a reasonable mechanism for the following reaction. Clearly show intermediates and show the movement of electron pairs with curved arrows. all сна H20. (H2SO4) H₃C CH₂ нас он H3CX сна 2. The addition of HBr to 2-methylpropene can, in principle, give either 1-bromo-2- methylpropane or 2-bromo-2-methylpropane. In reality, only the latter is formed. Show mechanisms...
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