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Advanced om 1) Name the following ethers (trum OH 2) Name the below molecule: OH 3)...
1) Name the following molecule: X OH 2) Draw the organic products formed in the following...
1) Name the following molecule: X OH 2) Draw the organic products formed in the following reactions. K₂Cr₂O7 H₂SO4, H₂o poh lohnen 3) Rank the following organic acids according to strength with 1 being the strongest acid. 4) Draw all resonance structures of the following deprotonated carboxylic acid:
1. Name the following or Draw the Structure (2 x 3 pts each) a. N-methyl-3-phenylpentan-2-amine OH...
1. Name the following or Draw the Structure (2 x 3 pts each) a. N-methyl-3-phenylpentan-2-amine OH b. OH NH2O 2. Draw the starting materials for the following hydrolysis reactions. (3 pts each) 1. NaOH, H2O a. 3-or 2. HCI, H2O OH OH Ph 1. NaOH, H2O b. HO Н. CH3 OH HPh 2. HCI, H2O 3. Of the following, which form would actually exist at: (5 points) a) pH = 2 (acidic) b) pH = 7 (neutral) c) pH =...
1) Name the following molecule: 2) Draw the organic products formed in the following reactions. K.C.07...
1) Name the following molecule: 2) Draw the organic products formed in the following reactions. K.C.07 H₂SO4, H₂o 3) Rank the following organic acids according to strength with 1 being the strongest acid 41 Draw il resonance structures of the fold r Carboxylic acids often exist as dimers, where two molecules are attached to each other Propose a reason. b. Draw an example of this phenomenon between two molecules of acetic acid (CH.COOH) Answer the following questions about the amino...
Question 11 2 pts What is the formal name for the molecule below: OH D Question...
Question 11 2 pts What is the formal name for the molecule below: OH D Question 12 What is the name of the functional group below: -CO-
Please help with all the parts! Question 3 (a) Name the following molecule: H3C OH CH3...
Please help with all the parts!
Question 3 (a) Name the following molecule: H3C OH CH3 a. [Marks: 11 i. If the all stereo centres are the R form; draw the Newman projection of the 3-4 bond of the molecule in part (a). ii. Using those projections sketch a rotational energy diagram for the conformers of the 3-4 bond. Assume that the highest steric/torsional strain is between the hydroxyl and vinyl groups [Marks: 3 (c) Show the mechanism for the...
a. Provide the IUPAC name of the molecule shown below. (4 points) b. Circle all achiral...
a. Provide the IUPAC name of the molecule shown below. (4 points) b. Circle all achiral (meso) compounds below. (4 points) OH COH HOZC OH c. Draw the structure of the compound based on its IUPAC name. (4 points) d. Of the cations below, circle any that are achiral. (4 points) OAC Hg ΤΗ (E)-4-ethyl-3-fluorohept-3-ene e. Provide the IUPAC name of the molecule shown below. (4 points) f Rank the following cations from least stable to most stable. (3 points)...
1) Draw the enol forms of the molecule shown here no OH 2) Provide the product...
1) Draw the enol forms of the molecule shown here no OH 2) Provide the product of each reaction shown below 1) NaNH2 CECH 2) 3) H20 2HCI o CECH - 1) NaNH2 Loech 1) HC =C 2) H20 1)BH3 2) H202/01 2 NaNH2 Bu Br. 3) Calculate the degree of hydrogen deficiency, also known as degre molecule with the formula C17H16F6N20 idea complete name that includes the E or Z descriptor for the allene hobe H2SO4 You Hoso. 1)...
PART A) Provide the major organic product of the reaction shown below. Draw the molecule on...
PART A) Provide the major organic product of the reaction shown
below.
Draw the molecule on the canvas by choosing buttons from the
Tools (for bonds), Atoms, and Advanced Template toolbars. The
single bond is active by default.
PART B)
Predict the starting materials necessary for the following
Robinson annulation.
Draw the molecules on the canvas by choosing buttons from the
Tools (for bonds), Atoms, and Advanced Template toolbars. The
single bond is active by default.
1. [(CH).СH],NLI 2. Н.С-СНCN...
6. Four part problem, all about the molecule shown in part a.) a.) Name the following...
6. Four part problem, all about the molecule shown in part a.) a.) Name the following molecule. OH b.) The alcohol could be converted into which of the functional groups below, using a reaction we have covered in this course (i.e., in one step)? Circle all correct answers. i.) carboxylic acid ii.) alkene iii.) ether iv.) ester v.) aldehyde vi.) epoxide vii.) ketone viii.) acetal c.) How many signals would be seen in the 'C NMR spectrum of the alcohol...
Which is the correct name for 1 a-3-iodopentan-2-al b-2-Iodopentan-3-one c-3-lodopentan-2-one 0-2-lodopentan-3-al Which is the correct name...
Which is the correct name for 1 a-3-iodopentan-2-al b-2-Iodopentan-3-one c-3-lodopentan-2-one 0-2-lodopentan-3-al Which is the correct name for a. 2-iodobutan-3-al b-3-jodobutan-2-one c-2-iodobutan-3-one d-3-iodobutan-2-al Which is the correct name for? a d-methylpropanal ethylpropanalb-propanone o-butanone 9. Which is the correct name for CH3CH2COCH2CH32 a diethyl ketone b-pentan-4-one c-pentan-3-ald-pentan-3-one e-pentan-2-one '' Which is the correct name for CH3CHO, a. Ethone b-ethanol c-vinger d-ketanal e-ethanal 11 ICH 2 -CH2-C-CH2-CH3 Which is the correct name for a. 5-jodopentan-2-one b- 1-iodopentan-2-one c-1-iodopentan-3-one d-5-iodopentan-3-one 12-Which of the following...
1) Name the following molecule: X OH 2) Draw the organic products formed in the following reactions. K₂Cr₂O7 H₂SO4, H₂o poh lohnen 3) Rank the following organic acids according to strength with 1 being the strongest acid. 4) Draw all resonance structures of the following deprotonated carboxylic acid:
1. Name the following or Draw the Structure (2 x 3 pts each) a. N-methyl-3-phenylpentan-2-amine OH b. OH NH2O 2. Draw the starting materials for the following hydrolysis reactions. (3 pts each) 1. NaOH, H2O a. 3-or 2. HCI, H2O OH OH Ph 1. NaOH, H2O b. HO Н. CH3 OH HPh 2. HCI, H2O 3. Of the following, which form would actually exist at: (5 points) a) pH = 2 (acidic) b) pH = 7 (neutral) c) pH =...
1) Name the following molecule: 2) Draw the organic products formed in the following reactions. K.C.07 H₂SO4, H₂o 3) Rank the following organic acids according to strength with 1 being the strongest acid 41 Draw il resonance structures of the fold r Carboxylic acids often exist as dimers, where two molecules are attached to each other Propose a reason. b. Draw an example of this phenomenon between two molecules of acetic acid (CH.COOH) Answer the following questions about the amino...
Question 11 2 pts What is the formal name for the molecule below: OH D Question 12 What is the name of the functional group below: -CO-
Please help with all the parts!
Question 3 (a) Name the following molecule: H3C OH CH3 a. [Marks: 11 i. If the all stereo centres are the R form; draw the Newman projection of the 3-4 bond of the molecule in part (a). ii. Using those projections sketch a rotational energy diagram for the conformers of the 3-4 bond. Assume that the highest steric/torsional strain is between the hydroxyl and vinyl groups [Marks: 3 (c) Show the mechanism for the...
a. Provide the IUPAC name of the molecule shown below. (4 points) b. Circle all achiral (meso) compounds below. (4 points) OH COH HOZC OH c. Draw the structure of the compound based on its IUPAC name. (4 points) d. Of the cations below, circle any that are achiral. (4 points) OAC Hg ΤΗ (E)-4-ethyl-3-fluorohept-3-ene e. Provide the IUPAC name of the molecule shown below. (4 points) f Rank the following cations from least stable to most stable. (3 points)...
1) Draw the enol forms of the molecule shown here no OH 2) Provide the product of each reaction shown below 1) NaNH2 CECH 2) 3) H20 2HCI o CECH - 1) NaNH2 Loech 1) HC =C 2) H20 1)BH3 2) H202/01 2 NaNH2 Bu Br. 3) Calculate the degree of hydrogen deficiency, also known as degre molecule with the formula C17H16F6N20 idea complete name that includes the E or Z descriptor for the allene hobe H2SO4 You Hoso. 1)...
PART A) Provide the major organic product of the reaction shown
below.
Draw the molecule on the canvas by choosing buttons from the
Tools (for bonds), Atoms, and Advanced Template toolbars. The
single bond is active by default.
PART B)
Predict the starting materials necessary for the following
Robinson annulation.
Draw the molecules on the canvas by choosing buttons from the
Tools (for bonds), Atoms, and Advanced Template toolbars. The
single bond is active by default.
1. [(CH).СH],NLI 2. Н.С-СНCN...
6. Four part problem, all about the molecule shown in part a.) a.) Name the following molecule. OH b.) The alcohol could be converted into which of the functional groups below, using a reaction we have covered in this course (i.e., in one step)? Circle all correct answers. i.) carboxylic acid ii.) alkene iii.) ether iv.) ester v.) aldehyde vi.) epoxide vii.) ketone viii.) acetal c.) How many signals would be seen in the 'C NMR spectrum of the alcohol...
Which is the correct name for 1 a-3-iodopentan-2-al b-2-Iodopentan-3-one c-3-lodopentan-2-one 0-2-lodopentan-3-al Which is the correct name for a. 2-iodobutan-3-al b-3-jodobutan-2-one c-2-iodobutan-3-one d-3-iodobutan-2-al Which is the correct name for? a d-methylpropanal ethylpropanalb-propanone o-butanone 9. Which is the correct name for CH3CH2COCH2CH32 a diethyl ketone b-pentan-4-one c-pentan-3-ald-pentan-3-one e-pentan-2-one '' Which is the correct name for CH3CHO, a. Ethone b-ethanol c-vinger d-ketanal e-ethanal 11 ICH 2 -CH2-C-CH2-CH3 Which is the correct name for a. 5-jodopentan-2-one b- 1-iodopentan-2-one c-1-iodopentan-3-one d-5-iodopentan-3-one 12-Which of the following...
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