The detail answers on the model 4 -electrophiles and the strength of the acid by their dissociation into the nature of the conjugated base were explained as below. All the sub parts of the three questions have been discussed as below.
I need help being walked through each part please lel 4: Electrophiles Il that an electrophile...
Explain what the double bond does to allow an alkene to act as a nucleophile. Select one: O a. The double bond acts as a Lewis base that can accept a proton b. The double bond acts as a Lewis base that can donate a proton O c. The double bond acts as a Lewis acid that can donate an electron d. The double bond acts as a Lewis base that can donate an electron pair e. The double bond...
9.1 Alcohols Worksheet Prior Knowledge: ✓ Acid/base definitions and pka values. ✓ Nucleophile/electrophile definitions and roles. ✓ Substitution and elimination reactions and mechanisms using curved arrows. Leaving group ability. Learning Objectives After completing this activity students should be able to: ✓ Predict the role of an alcohol in the Williamson Ether Synthesis and Fisher Esterification. Determine that protonation of an alcohol affords stronger electrophiles because of better, more stabilized, leaving groups. Conversion of Alcohols to Electrophiles Protonation RCH,OH + H...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
please help
4. For each pair of structures below circle the most relatively stable one. Show work by drawing relevant chair structures and/or Newman projections as needed) to clearly illustrate why. It is best practice here that only the most stable conformations for each compound are being compared in each set. For clarity. provide a few words that explain your analysis when comparing the illustrations. (12pts total for this problem) (a) ♡ va ♡ 5. (a) (3pts) Look up trans-decalin...
Please help with questions 1-5. I have attached the additional
lab information pages for help if you are unclear on anything
please review those.
We were unable to transcribe this imageEAS 97 5. Calculate the theoretical yiel te the theoretical yield of iodinated salicylamide (product) ass Todination reaction. (Show your calculations.) mide (product) assuming a mono- le, your starting material, is shown in Figure 4. ces in the functional group region of the spectrum IR spectrum of salicylamide, your starting...
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need help with the excercises listed on the first page: 18 and
19
18. Complete each of the following reactions. Then determine where the equilibrium is moving it is say which one favors the formation of the reactants and which one favors the formation of the products. If you cannot decide with the structure, compare the pka value of the acid with that of the conjugate acid. 4. CHỊCH NH • Hỏi - CHCH-CC-H.H c. CHOH + H-Br =...
please help! correlation of acidity with electrostatic
potential. The assigned acid is Maleic Acid: Electrostatic
Potential is 379.2 kJ/mol. Answering any part of this assignment
would help greatly to understand more about it.
Assigned Acid #27 03 02 04 01 C2. H3 H2 Maleic Acid - Electrostatic Potential is 379.2 k]/mol Kal = 1.2 x 102 1. Using the Electrostatic Potential Map word document posted on Moodle, identify the region(s) with the most positive electrostatic potential of your assigned acid...
For
letters h & i :
For each of the following reactions, predict the major
mechanistic pathway (SN1/SN2/E1/E2) and the major organic
products
1. (cont.) (h) НСОН CHB -CHBr HCOH - (0) CH,CH,CH,CH,Br- NH 2. For each of the following indicate which reaction will occur faster. Explain your reasoning. (No credit will be given for guesses) (a) The reaction of (CH),CBr with 0.001M aqueous NaOH or 0.10M aqueous NaOH (b) The reaction of 2-bromobutane with NaOH in DMSO or NaSH...
1-24 need help really lost
Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for the following deprotonation step. Also add the other product notice how the Tema s can be converted to this by use of a strong base such as sodium a sodium ion (Na) is not drawn, in this case it is just a spectatorio PCW27 - Mechanistic steps - Part Name: Time spent 2) Label the above compounds with the appropriate name from the previous...
please I need help with the data sheet
INTRODUCTION The chemical and physical properties of substances are influenced by the way in which valence electrons are distributed and by the three-dimensional shape of the molecule or ion. X- ray and neutron diffraction, infrared, Raman and microwave absorption spectroscopy, as well as dipole moment measurements are used to ascertain the three-dimensional structure of a substance. Thus, techniques are available which can identify the geometry of substances. Results of these measurements generally...