Please explain how to approach solving this problem and how to get the correct solution. I know the little triangle above the arrow means its being heated. Thank you so much in advance.
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Please explain how to approach solving this problem and how to
get the correct solution. I...
I. (40 points) Predict the major product(s) for each of the following transformations. Be sure to...
I. (40 points) Predict the major product(s) for each of the following transformations. Be sure to indicate stereochemistry and draw enantiomers when appropriate. Clearly show stereochemistry with two lines in the plane and a wedge or dash at the chirality center. No reaction mechanisms are necessary.
2 Prelaboratory Assignment (Due at the beginning of lab) 1. Predict the major product(s) for the...
2 Prelaboratory Assignment (Due at the beginning of lab) 1. Predict the major product(s) for the following reactions wedge and/or dash at the chirality center. No reaction mechani Be sure to indicate s wedge andlor dash at then appropriate. Show stereochemistry with two lines in the plane and a H20 + HO- (in excess; used as solvent) H20 (in excess: used as solvent) くへ人。ヘ HO- но- +
please do all of 1 and please explain number 2, I dont understand. 1. a. (4...
please do all of 1 and please explain number 2, I dont
understand.
1. a. (4 points) Draw the dash-wedge structure of (2,3S)-2,3-dichloropentane. b. (4 points) Draw the Fischer projection of enantiomer of the compound drawn in part a. Name the enantiomers. c. (6 points) Draw the Newman projections (looking down the C2-C3 bonds) of the diastereomers of the compound drawn in part b. Name the diastereomers. 2. (6 points) Draw the mechanisms of the propagation steps of the reaction...
Please explain how you approach this so I can emulate your problem solving strategies on like...
Please explain how you approach this so I can emulate your
problem solving strategies on like problems
Suppose we had a large, positively charged plate in an upright (vertical) position and a point charge with positive charge +Q. In lecture, you saw that a large charged plate gives rise to an electric field which is constant in space: we will call this electric field Eplate. Let us suppose also that we had a s bl with positive charge +q and...
Chiral catalysts can be designed to favor the formation of one enantiomer over another in reactions...
Chiral catalysts can be designed to favor the formation of one enantiomer over another in reactions where a new chiral center is formed. The example shown below was recently reported in the chemical literature (J. Am. Chem. Soc. 2012. 134, 8054 8057) where a new type of chiral copper (Cu) catalyst was developed. When the Cul catalyst was used, the (S)-enantiomer of the product predominated, and the (R)-enantiomer of the product was selectively formed when Cu" catalyst was used instead....
4. Chiral catalysts can be designed to favor the formation of one enantiomer over another in...
4. Chiral catalysts can be designed to favor the formation of one enantiomer over another in reactions where a new chiral center is formed. The example shown below was recently reported in the chemical literature (J. Am. Chem. Soc. 2012, 134, 8054-8057) where a new type of chiral copper (Cu) catalyst was developed. When the Cu' catalyst was used, the (S)-enantiomer of the product predominated, and the (R)-enantiomer of the product was selectively formed when Cu" catalyst was used instead....
PLEASE READ THIS BEFORE YOU START SOLVING: I need an explanation for Part d only. The correct answer is 4.02 m, but I don't know how to get it, thanks! No need to do parts a, b and c!! THANK YOUU...
PLEASE READ THIS
BEFORE YOU START SOLVING: I need an explanation for Part
d only. The correct answer is 4.02 m, but I don't know how to get
it, thanks! No need to do parts a, b and c!! THANK
YOUUUUU
Free Surface A curved surface as shown in the diagram above) defined as a quarter circle with radius of length r = 18 m is submerged in a liquid with the flat edge at a distance h - 10...
PLEASE HELP WITH THESE. THANK YOU How are the following two compounds related? CH CH3 HO...
PLEASE HELP WITH THESE. THANK
YOU
How are the following two compounds related? CH CH3 HO -H HO -Н Given the following substitution reaction, what would the effect be of changing the solvent from CH3OH to (CH3)2S=0? H- OH H OH VS HO -H H -OH H -OH HO H + CH (CH2CH2-Br NaOH CH;(CH2), CH2-OH + NaBr CH OH CH2OH A. The reaction rate will increase. OB. There is no effect on the rate of the reaction, C. The...
could you please help me with this problem, also I need a little text so I...
could you please help me with this problem, also I
need a little text so I can understand how you solved the
problem?
import java.io.File; import java.util.Scanner; /** *
This program lists the files in a directory specified by * the
user. The user is asked to type in a directory name. * If the name
entered by the user is not a directory, a * message is printed and
the program ends. */ public class DirectoryList { public static...
I need help with my very last assignment of this term PLEASE!!, and here are the instructions: After reading Chapter T...
I need help with my very last assignment of this term
PLEASE!!, and here are the instructions: After reading Chapter Two,
“Keys to Successful IT Governance,” from Roger Kroft and Guy
Scalzi’s book entitled, IT Governance in Hospitals and Health
Systems, please refer to the following assignment instructions
below.
This chapter consists of interviews with executives
identifying mistakes that are made when governing healthcare
information technology (IT). The chapter is broken down into
subheadings listing areas of importance to understand...
I. (40 points) Predict the major product(s) for each of the following transformations. Be sure to indicate stereochemistry and draw enantiomers when appropriate. Clearly show stereochemistry with two lines in the plane and a wedge or dash at the chirality center. No reaction mechanisms are necessary.
2 Prelaboratory Assignment (Due at the beginning of lab) 1. Predict the major product(s) for the following reactions wedge and/or dash at the chirality center. No reaction mechani Be sure to indicate s wedge andlor dash at then appropriate. Show stereochemistry with two lines in the plane and a H20 + HO- (in excess; used as solvent) H20 (in excess: used as solvent) くへ人。ヘ HO- но- +
please do all of 1 and please explain number 2, I dont
understand.
1. a. (4 points) Draw the dash-wedge structure of (2,3S)-2,3-dichloropentane. b. (4 points) Draw the Fischer projection of enantiomer of the compound drawn in part a. Name the enantiomers. c. (6 points) Draw the Newman projections (looking down the C2-C3 bonds) of the diastereomers of the compound drawn in part b. Name the diastereomers. 2. (6 points) Draw the mechanisms of the propagation steps of the reaction...
Please explain how you approach this so I can emulate your
problem solving strategies on like problems
Suppose we had a large, positively charged plate in an upright (vertical) position and a point charge with positive charge +Q. In lecture, you saw that a large charged plate gives rise to an electric field which is constant in space: we will call this electric field Eplate. Let us suppose also that we had a s bl with positive charge +q and...
Chiral catalysts can be designed to favor the formation of one enantiomer over another in reactions where a new chiral center is formed. The example shown below was recently reported in the chemical literature (J. Am. Chem. Soc. 2012. 134, 8054 8057) where a new type of chiral copper (Cu) catalyst was developed. When the Cul catalyst was used, the (S)-enantiomer of the product predominated, and the (R)-enantiomer of the product was selectively formed when Cu" catalyst was used instead....
4. Chiral catalysts can be designed to favor the formation of one enantiomer over another in reactions where a new chiral center is formed. The example shown below was recently reported in the chemical literature (J. Am. Chem. Soc. 2012, 134, 8054-8057) where a new type of chiral copper (Cu) catalyst was developed. When the Cu' catalyst was used, the (S)-enantiomer of the product predominated, and the (R)-enantiomer of the product was selectively formed when Cu" catalyst was used instead....
PLEASE READ THIS
BEFORE YOU START SOLVING: I need an explanation for Part
d only. The correct answer is 4.02 m, but I don't know how to get
it, thanks! No need to do parts a, b and c!! THANK
YOUUUUU
Free Surface A curved surface as shown in the diagram above) defined as a quarter circle with radius of length r = 18 m is submerged in a liquid with the flat edge at a distance h - 10...
PLEASE HELP WITH THESE. THANK
YOU
How are the following two compounds related? CH CH3 HO -H HO -Н Given the following substitution reaction, what would the effect be of changing the solvent from CH3OH to (CH3)2S=0? H- OH H OH VS HO -H H -OH H -OH HO H + CH (CH2CH2-Br NaOH CH;(CH2), CH2-OH + NaBr CH OH CH2OH A. The reaction rate will increase. OB. There is no effect on the rate of the reaction, C. The...
could you please help me with this problem, also I
need a little text so I can understand how you solved the
problem?
import java.io.File; import java.util.Scanner; /** *
This program lists the files in a directory specified by * the
user. The user is asked to type in a directory name. * If the name
entered by the user is not a directory, a * message is printed and
the program ends. */ public class DirectoryList { public static...
I need help with my very last assignment of this term
PLEASE!!, and here are the instructions: After reading Chapter Two,
“Keys to Successful IT Governance,” from Roger Kroft and Guy
Scalzi’s book entitled, IT Governance in Hospitals and Health
Systems, please refer to the following assignment instructions
below.
This chapter consists of interviews with executives
identifying mistakes that are made when governing healthcare
information technology (IT). The chapter is broken down into
subheadings listing areas of importance to understand...
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