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E See page 188 17 Question (1 point) The structure of a trisubstituted cyclohexane is shown,...
3. (1 pt.) Draw the most stable chair conformation for the following trisubstituted cyclohexane (write letters...
3. (1 pt.) Draw the most stable chair conformation for the following trisubstituted cyclohexane (write letters a (axial), elequatorial), d(down), u(up)) next to each substituent to indicate is position in the ring. 1112 COOH
Draw (S,E)-1-(methylamino) but-2-en-1-ol Question (1 point) G See page 387 19 Draw (SE)-1-(methylamino)but-2-en-1-ol. 4th attempt See...
Draw (S,E)-1-(methylamino) but-2-en-1-ol
Question (1 point) G See page 387 19 Draw (SE)-1-(methylamino)but-2-en-1-ol. 4th attempt See Hint atd See Periodic Table Please draw all four bonds at chiral centers. Use wedge and dash bonds at chiral centers only. Do not use wedges and dashes at non- chiral centers.
Pleqsw help with this question 3. (a) Consider the bond-line (dash/wedge) structure shown below. Using the...
Pleqsw help with this question
3. (a) Consider the bond-line (dash/wedge) structure shown below. Using the Newman projection templates provided to the right of this bond-line structure, draw the overall lowest energy (most stable) and overall highest energy (least stable) conformation possible in Newman projection form sighting down the C C, bond indicated. Provide a one sentence explanation to justify for the overall most stable conformation. (Ipts each correct Newman, 2pts for valid explanation) sight down Cy-- - bond .23...
4. a) Draw the perspective (dashes and wedges) structure of an androstane analog comprised of acarbonyl group at C-3, a carboxylic acid group at C-17 and a double bond between C-5 and C-6; whatkind of...
4. a) Draw the perspective (dashes and wedges) structure of an androstane analog comprised of acarbonyl group at C-3, a carboxylic acid group at C-17 and a double bond between C-5 and C-6; whatkind of lipid is this? b) Draw the perspective structure of the products of its reaction with 1) bromine followed by 2) water;assign R and S to all chiral centers. (Also consider whether these reagents react with the carbonyl and and/or the carboxylic acid group/s; can an...
Procedure B. 1. Build two models of 1, 2-dimethyleyclopentane. The two methy can be on the...
Procedure B. 1. Build two models of 1, 2-dimethyleyclopentane. The two methy can be on the same face or opposite faces of the ring. No matter how t molecule is twisted, they cannot be superimposed on each other. These compounds are stereoisomers of each other. 2. When two groups are present, the prefix cis (same face) or trans (opposite face) can be used in IUPAC nomenclature to specify which stereoisomer is being considered. For drawings, a solid wedged line in...
Key concepts: molecular represenations, stereolsomers, RS enantiomeric excess, IPAC naming covention Provide the IUPAC name for...
Key concepts: molecular represenations, stereolsomers, RS enantiomeric excess, IPAC naming covention Provide the IUPAC name for each of the following molecules 0% HJC BM How similar are the names for B and C, even though there is the single change to the structure 2 Rank the priorities of these functional groups and substituents using Cahn-Ingold-Prelog nomenclature. Highest priority will be 1 and lowest will be 5; show your rationale CH:CH:CH CH CHCH:CH CHs,-SCH,-CH: CH:CH:CHCH CHCH, -CH2NHOH,-CH:NO Draw dash/wedge representations for...
Name: Integumentary System Case Study: Jon's Story (Each question is worth 0.5 pts) At 63 years...
Name: Integumentary System Case Study: Jon's Story (Each question is worth 0.5 pts) At 63 years old, Jon was retiring early by most people's standards, but he felt it was time and he was looking forward to it. His mind wandered as he raked the dry remnants of his front yard. The African summer had been hotter than usual but he had always worked outdoors and the warmth of the sun on his face felt good. Jon had grown up...
10. Write a one-page summary of the attached paper? INTRODUCTION Many problems can develop in activated...
10. Write a one-page summary of the attached paper? INTRODUCTION Many problems can develop in activated sludge operation that adversely affect effluent quality with origins in the engineering, hydraulic and microbiological components of the process. The real "heart" of the activated sludge system is the development and maintenance of a mixed microbial culture (activated sludge) that treats wastewater and which can be managed. One definition of a wastewater treatment plant operator is a "bug farmer", one who controls the aeration...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23,...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
Hi there! I need to compare two essay into 1 essay, and make it interesting and...
Hi there! I need to compare two essay into 1 essay, and make it interesting and choose couple topics which im going to talk about in my essay FIRST ESSAY “Teaching New Worlds/New Words” bell hooks Like desire, language disrupts, refuses to be contained within boundaries. It speaks itself against our will, in words and thoughts that intrude, even violate the most private spaces of mind and body. It was in my first year of college that I read Adrienne...
3. (1 pt.) Draw the most stable chair conformation for the following trisubstituted cyclohexane (write letters a (axial), elequatorial), d(down), u(up)) next to each substituent to indicate is position in the ring. 1112 COOH
Draw (S,E)-1-(methylamino) but-2-en-1-ol
Question (1 point) G See page 387 19 Draw (SE)-1-(methylamino)but-2-en-1-ol. 4th attempt See Hint atd See Periodic Table Please draw all four bonds at chiral centers. Use wedge and dash bonds at chiral centers only. Do not use wedges and dashes at non- chiral centers.
Pleqsw help with this question
3. (a) Consider the bond-line (dash/wedge) structure shown below. Using the Newman projection templates provided to the right of this bond-line structure, draw the overall lowest energy (most stable) and overall highest energy (least stable) conformation possible in Newman projection form sighting down the C C, bond indicated. Provide a one sentence explanation to justify for the overall most stable conformation. (Ipts each correct Newman, 2pts for valid explanation) sight down Cy-- - bond .23...
Procedure B. 1. Build two models of 1, 2-dimethyleyclopentane. The two methy can be on the same face or opposite faces of the ring. No matter how t molecule is twisted, they cannot be superimposed on each other. These compounds are stereoisomers of each other. 2. When two groups are present, the prefix cis (same face) or trans (opposite face) can be used in IUPAC nomenclature to specify which stereoisomer is being considered. For drawings, a solid wedged line in...
Key concepts: molecular represenations, stereolsomers, RS enantiomeric excess, IPAC naming covention Provide the IUPAC name for each of the following molecules 0% HJC BM How similar are the names for B and C, even though there is the single change to the structure 2 Rank the priorities of these functional groups and substituents using Cahn-Ingold-Prelog nomenclature. Highest priority will be 1 and lowest will be 5; show your rationale CH:CH:CH CH CHCH:CH CHs,-SCH,-CH: CH:CH:CHCH CHCH, -CH2NHOH,-CH:NO Draw dash/wedge representations for...
Name: Integumentary System Case Study: Jon's Story (Each question is worth 0.5 pts) At 63 years old, Jon was retiring early by most people's standards, but he felt it was time and he was looking forward to it. His mind wandered as he raked the dry remnants of his front yard. The African summer had been hotter than usual but he had always worked outdoors and the warmth of the sun on his face felt good. Jon had grown up...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
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