in the cyclohexane template provided
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in the cyclohexane template provided
In the cyclohexane template provided, click on all the substituents (F,...
Given the planar trisubstituted cyclohexane below, fill in all boxes (with H, F,Cl or Br) to...
Given the planar trisubstituted cyclohexane below, fill in all boxes (with H, F,Cl or Br) to complete the two possible cyclohexane chair conformations.
Which is the more stable conformer?
Chair1
Chair2
Remove one hydrogen atom from C_1 the hexane model, and one H atom plus its bond...
Remove one hydrogen atom from C_1 the hexane model, and one H atom plus its bond from C_6. Bend the carbon chain around and join C_1 to C_6 to make cyclohexane. Mentally designate one carbon as C_1. Place the model in the chair conformation by tipping C_1 up and C_4 down. Check the conformation with the instructor. Identify the axial and equatorial hydrogens and describe their orientation relative to the plane of the ring. Look down each successive C-C bond...
Part 2: Substituted Hydrocarbons View the first compound structure provided in Table 5. Follow the steps...
Part 2: Substituted Hydrocarbons
View the first compound structure provided in Table 5. Follow
the steps below and write each part of the name on a piece of
paper.
Identify the parent chain of the compound.
Count the number of carbon atoms and determine the type of
carbon-carbon bonds (single, double, or triple) to record the base
name of the compound with the correct suffix.
Number the carbons by beginning on the end with the closest
substituent(s) for single bonded...
Help Organic Chem part 7 Do the two examples by drawing the perspective drawings in the...
Help Organic Chem part 7
Do the two examples by drawing the perspective drawings in the
box. And include the angle.
Perspective drawings (Haworth projections) Cyclic structures can be described using bond-line drawings, but can also be drawn using perspective drawings (Haworth Projections), which are used very often in biochemistry. In perspective drawings, the ring is viewed from a "side perspective" and the substituents are drawn pointing either straight up or straight down. cyclobutane (C4H3) cyclohexane (C6H12) Wedge-Dash drawing Perspective...
Consider the function f(x) = 23 +22 - 22 Answer all parts: (a) - (f). (a)...
Consider the function f(x) = 23 +22 - 22 Answer all parts: (a) - (f). (a) What is the degree of f(c)? The degree of f(x) is (b) Which of the following choices describe the end behavior of f(c)? The graph of f(x) acts O like 22 (i.e. both ends up) O like -2- (.e. both ends down) O like x3 (ie, left end down, right end up) O like 1-3 (.e. left end up, right end down) O None...
Consider the function f(x) = 24 - 73 - 6.22 Answer all parts: (a)-(t). (a) What...
Consider the function f(x) = 24 - 73 - 6.22 Answer all parts: (a)-(t). (a) What is the degree of f(x)? The degree of f(u) is (b) Which of the following choices describe the end behavior of f(x)? Olike 2 The graph of f(x) acts (i.e. both ends up) O like ---2 (ie, both ends down) Lake 3 (ie left end down right end up) like - 3 (ie left end up, right end down) O None of the above...
Consider the DList class provided in the Week 6 source code archive which stored int data. A common operation on a DList object list is to make a copy or clone of list. For example, DList list n...
Consider the DList class provided in the Week 6 source code archive which stored int data. A common operation on a DList object list is to make a copy or clone of list. For example, DList list new DList /I code is here that adds data to list so list is now (1, 2, 3, 4, 5) DList clone = list.clone ( ); // clone is an entirely separate list with the same values as list, İ.e., the /I contents...
Select all of the carbons in the structure below to which bromine can become attached upon...
Select all of the carbons in the structure below to
which bromine can become attached upon reaction of the alkene with
NBS.
When the alkene below is brominated with NBS reaction can occur at more than one carbon. Select all of the carbons in the structure below to which bromine can become attached upon reaction of the alkene with NBS Gray C; white = H; red O; blue = N; dark green Cl; brown - Br; light green F; purple...
Answer H has been provided, please show work for your steps to the solutions Choose a...
Answer H has been provided, please show work for your steps to
the solutions
Choose a coordinate system. 5. What is the electric field at point P due to the ring Segment i with charge Divide the ring into segments. of charge Q? We'll do the same steps. Use the coordinate system given. The ring has radius R, is in the xy plane, and the point is a horizontal distance - away on the - axis. 2 Identify the a)...
A. Which of the following Newman projections would represent the least stable conformer of 2,2,3....
PLEASE HELP WITH ALL.
A. Which of the following Newman projections would represent the least stable conformer of 2,2,3.3-tetramethylbutane, looking down the 2,3 bond? H3C H3C H3C H3C CH3 b) CH3 H3C e) a) c) CH3 H3C CH3 CH CH3 CH о он B. which one of the following compounds would be chiral? Br он о он a) но HO O он HO C C. which of the following could potentially be used to distinguish between enantiomers? b) NMR c)...
Given the planar trisubstituted cyclohexane below, fill in all boxes (with H, F,Cl or Br) to complete the two possible cyclohexane chair conformations.
Which is the more stable conformer?
Chair1
Chair2
Remove one hydrogen atom from C_1 the hexane model, and one H atom plus its bond from C_6. Bend the carbon chain around and join C_1 to C_6 to make cyclohexane. Mentally designate one carbon as C_1. Place the model in the chair conformation by tipping C_1 up and C_4 down. Check the conformation with the instructor. Identify the axial and equatorial hydrogens and describe their orientation relative to the plane of the ring. Look down each successive C-C bond...
Part 2: Substituted Hydrocarbons
View the first compound structure provided in Table 5. Follow
the steps below and write each part of the name on a piece of
paper.
Identify the parent chain of the compound.
Count the number of carbon atoms and determine the type of
carbon-carbon bonds (single, double, or triple) to record the base
name of the compound with the correct suffix.
Number the carbons by beginning on the end with the closest
substituent(s) for single bonded...
Help Organic Chem part 7
Do the two examples by drawing the perspective drawings in the
box. And include the angle.
Perspective drawings (Haworth projections) Cyclic structures can be described using bond-line drawings, but can also be drawn using perspective drawings (Haworth Projections), which are used very often in biochemistry. In perspective drawings, the ring is viewed from a "side perspective" and the substituents are drawn pointing either straight up or straight down. cyclobutane (C4H3) cyclohexane (C6H12) Wedge-Dash drawing Perspective...
Consider the function f(x) = 23 +22 - 22 Answer all parts: (a) - (f). (a) What is the degree of f(c)? The degree of f(x) is (b) Which of the following choices describe the end behavior of f(c)? The graph of f(x) acts O like 22 (i.e. both ends up) O like -2- (.e. both ends down) O like x3 (ie, left end down, right end up) O like 1-3 (.e. left end up, right end down) O None...
Consider the function f(x) = 24 - 73 - 6.22 Answer all parts: (a)-(t). (a) What is the degree of f(x)? The degree of f(u) is (b) Which of the following choices describe the end behavior of f(x)? Olike 2 The graph of f(x) acts (i.e. both ends up) O like ---2 (ie, both ends down) Lake 3 (ie left end down right end up) like - 3 (ie left end up, right end down) O None of the above...
Consider the DList class provided in the Week 6 source code archive which stored int data. A common operation on a DList object list is to make a copy or clone of list. For example, DList list new DList /I code is here that adds data to list so list is now (1, 2, 3, 4, 5) DList clone = list.clone ( ); // clone is an entirely separate list with the same values as list, İ.e., the /I contents...
Select all of the carbons in the structure below to
which bromine can become attached upon reaction of the alkene with
NBS.
When the alkene below is brominated with NBS reaction can occur at more than one carbon. Select all of the carbons in the structure below to which bromine can become attached upon reaction of the alkene with NBS Gray C; white = H; red O; blue = N; dark green Cl; brown - Br; light green F; purple...
Answer H has been provided, please show work for your steps to
the solutions
Choose a coordinate system. 5. What is the electric field at point P due to the ring Segment i with charge Divide the ring into segments. of charge Q? We'll do the same steps. Use the coordinate system given. The ring has radius R, is in the xy plane, and the point is a horizontal distance - away on the - axis. 2 Identify the a)...
PLEASE HELP WITH ALL.
A. Which of the following Newman projections would represent the least stable conformer of 2,2,3.3-tetramethylbutane, looking down the 2,3 bond? H3C H3C H3C H3C CH3 b) CH3 H3C e) a) c) CH3 H3C CH3 CH CH3 CH о он B. which one of the following compounds would be chiral? Br он о он a) но HO O он HO C C. which of the following could potentially be used to distinguish between enantiomers? b) NMR c)...
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