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can all parts of question A be answered and labeled please.
there is no data for...
can question A parts A4 (a and b) A5 and A6 be answered neatly and labled....
can question A parts A4 (a and b) A5 and A6 be answered neatly
and labled. with specifics in A5 and A6
Dale Tepot sub Partners NUCLEOPHILIC SUBSTITUTION A. Structural Effects on Sn1 and Sn2 Reactivity A1. In the following table, record the results of your group's experiments with the five alkyl halides and the two reagents, sodium iodide in acetone and alcoholic silver nitrate. Note the elapsed time required for turbidity to appear and for a precipitate to form....
can question A2 part a and b be answered and labeled please. information has been provided....
can question A2 part a and b be answered and labeled please.
information has been provided.
NUCLEOPHILIC SUBSTITUTION A. Structural Effects on S, 1 and S 2 Reactivity Al. In the following table, record the results of your group's experiments with the five alkyl halides and the two reagents, sodium iodide in acetone and alcoholic silver nitrate. Note the elapsed time required for turbidity to appear and for a precipitate to form. I you heated any of the test tubes,...
can question B of B2 and B3 be answered please. information has also been provided B....
can
question B of B2 and B3 be answered please.
information has also been provided
B. Effect of Solvent on SN1 Reactivity B1. In 1. In the following table, record the time in seconds required for the pink color to disappear in each solvent mixture. Compositon (solvent:water) Reaction time in seconds Methanol Ethanol Acetone 6:175 non reachre 2:405 1.1 mL:0.9 mL (55:45) 1.2 mL:0.8 mL (60:40) 1.3 mL:0.7 mL (65:35) 1.4 mL:0.6 mL (70:30) 7:32 5 08 s 6:49 5:475...
We begin with the surmise that the nucleophilic substitution reactions can occur only by one of...
We begin with the surmise that the nucleophilic substitution reactions can occur only by one of two mechanisms: Sn1 solvolysis: three-step mechanism R-X slow, R® + to R® + ROH fast , ROM R' H. R-O + R'OH fast , ROR' + R- SN2: one-step mechanism R-X + Nuc slow, Nuc-R + x Begin by answering the three questions below. If you don't understand what's up, please ask! 1. Write out the rate law for the above Sn1 reaction and...
Draw the strcture of all substrates you will be using in this reaction and classify them...
Draw the strcture of all substrates you will be using in this
reaction and classify them as( primary, Secondary, and tertiary)
aryl bezylic or some combination of these (such as primary
bezylic). Identify the nucleophile, substrate, and leaving group in
general equations for reactions 1 and 2
ORRAS sminilah you dimensions (R) or (S), and show their stereochemistry clearly. If your instructor reguests, obtain another set of atoms and connectors and use it to prepare isomers as well. R eal...
Can you please answer all of them? Section B: Free Response (you must show your work...
Can you please answer all of them?
Section B: Free Response (you must show your work for full credit) 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect...
2) Predict the order of reactivity (1=least, 4=most) of primary, secondary, tertiary, and aryl halides toward...
2) Predict the order of reactivity (1=least, 4=most) of
primary, secondary, tertiary, and aryl halides toward nucleophilic
displacement by an SN1 reaction mechanism. Explain
3) Give a detailed summary of the chemistry in both reactions
SN2 and SN1 in details please for both reactions. include any
general statements about the experiments.
LAB)o Organic Chemistry I Lab CHEM 3512 Nueleophilic Substitution Reactions: Sl vs S2 To review Sul, S2, El and E2 reactions and mechanisms and compare and contrast the effect...
Please give detailed answers to the pre and post lab questions. Thank you! NUCLEOPHILIC DISPLACEMENT- FORMATION...
Please give detailed answers to the pre and post lab questions.
Thank you!
NUCLEOPHILIC DISPLACEMENT- FORMATION OF AN ETHER BY AN SN2 REACTION Bond formation by use of an SN2 reaction is very important for organic and biological synthesis. Many new bonds formed make use of this versatile reaction pathway. In this reaction, one partner is the nucleophile and the other partner is the electrophile. The electrophile will have a leaving group that will be lost in the reaction. In...
Can you please help me with this question. Much appreciated. So I have a sample code,...
Can you please help me with this question. Much appreciated. So
I have a sample code, but we need to change the code in a way that
fits the problem.
A planar slab of material is initially at a temperature of 300 K. At the time t=0, microwave radiation is directed at the material, leading to internal heat generation that is uniform within the material. The sides of the slab experience negligible heat losses and a water bath maintains the...
show all calculations and do all parts of the question. Externalities II [Warning, this problem is...
show all calculations and do all parts of the question. Externalities II [Warning, this problem is an enhanced version of a negative externality problem. While I break it down into a series of short steps, it still may take a long time to figure out. Budget accordingly. Don’t skimp on your graph. Your picture will hopefully help you understand what is going on.] High levels of automobile traffic in big cities are incredibly costly to society. Time spent idling in...
can question A parts A4 (a and b) A5 and A6 be answered neatly
and labled. with specifics in A5 and A6
Dale Tepot sub Partners NUCLEOPHILIC SUBSTITUTION A. Structural Effects on Sn1 and Sn2 Reactivity A1. In the following table, record the results of your group's experiments with the five alkyl halides and the two reagents, sodium iodide in acetone and alcoholic silver nitrate. Note the elapsed time required for turbidity to appear and for a precipitate to form....
can question A2 part a and b be answered and labeled please.
information has been provided.
NUCLEOPHILIC SUBSTITUTION A. Structural Effects on S, 1 and S 2 Reactivity Al. In the following table, record the results of your group's experiments with the five alkyl halides and the two reagents, sodium iodide in acetone and alcoholic silver nitrate. Note the elapsed time required for turbidity to appear and for a precipitate to form. I you heated any of the test tubes,...
can
question B of B2 and B3 be answered please.
information has also been provided
B. Effect of Solvent on SN1 Reactivity B1. In 1. In the following table, record the time in seconds required for the pink color to disappear in each solvent mixture. Compositon (solvent:water) Reaction time in seconds Methanol Ethanol Acetone 6:175 non reachre 2:405 1.1 mL:0.9 mL (55:45) 1.2 mL:0.8 mL (60:40) 1.3 mL:0.7 mL (65:35) 1.4 mL:0.6 mL (70:30) 7:32 5 08 s 6:49 5:475...
We begin with the surmise that the nucleophilic substitution reactions can occur only by one of two mechanisms: Sn1 solvolysis: three-step mechanism R-X slow, R® + to R® + ROH fast , ROM R' H. R-O + R'OH fast , ROR' + R- SN2: one-step mechanism R-X + Nuc slow, Nuc-R + x Begin by answering the three questions below. If you don't understand what's up, please ask! 1. Write out the rate law for the above Sn1 reaction and...
Draw the strcture of all substrates you will be using in this
reaction and classify them as( primary, Secondary, and tertiary)
aryl bezylic or some combination of these (such as primary
bezylic). Identify the nucleophile, substrate, and leaving group in
general equations for reactions 1 and 2
ORRAS sminilah you dimensions (R) or (S), and show their stereochemistry clearly. If your instructor reguests, obtain another set of atoms and connectors and use it to prepare isomers as well. R eal...
Can you please answer all of them?
Section B: Free Response (you must show your work for full credit) 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect...
2) Predict the order of reactivity (1=least, 4=most) of
primary, secondary, tertiary, and aryl halides toward nucleophilic
displacement by an SN1 reaction mechanism. Explain
3) Give a detailed summary of the chemistry in both reactions
SN2 and SN1 in details please for both reactions. include any
general statements about the experiments.
LAB)o Organic Chemistry I Lab CHEM 3512 Nueleophilic Substitution Reactions: Sl vs S2 To review Sul, S2, El and E2 reactions and mechanisms and compare and contrast the effect...
Please give detailed answers to the pre and post lab questions.
Thank you!
NUCLEOPHILIC DISPLACEMENT- FORMATION OF AN ETHER BY AN SN2 REACTION Bond formation by use of an SN2 reaction is very important for organic and biological synthesis. Many new bonds formed make use of this versatile reaction pathway. In this reaction, one partner is the nucleophile and the other partner is the electrophile. The electrophile will have a leaving group that will be lost in the reaction. In...
Can you please help me with this question. Much appreciated. So
I have a sample code, but we need to change the code in a way that
fits the problem.
A planar slab of material is initially at a temperature of 300 K. At the time t=0, microwave radiation is directed at the material, leading to internal heat generation that is uniform within the material. The sides of the slab experience negligible heat losses and a water bath maintains the...
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