Reaction mechanism:
1) In HBr addition of alkene the bromide ion end up with more substituted carbon. This reaction follows Morkonikov rule.
2) Alkene react with Br2 molecule gives bromonium ion intermediate then solvent water molecule act as nucleophile and attack gives bromo hydrine. The bromonium ion ring opening follows SN2 mechanism so both Br an OH are opposite plane in the product.
3) Simmons smith reaction conditions convert the alkene into cyclopropane.
4) The alkyne converted into aldehyde by Hydroboration followed by peroxide oxidation.
please help me complete the transformations shown and if you van include the missing thing jn...
Complete the following transformations. From Br - To: Et = Me Rr CHCI From HH ен, CH3CI CHCI: o Design syntheses of compound A. The pool of carbon- containing starting materials that you can use are shown in the square brackets. You may use any common reagents. Br HC CH hy
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2. a) Use transformations of the graph of y = 2* to graph y = 2x+2. -2 -5 b) Write the domain and range in interval and set-builder notation. c) Write an equation of the asymptote.
C++ assignment. Please help me to complete this code: #include <string> #include <iostream> using namespace std; // Write your function here //////////////// STUDENT TESTING //////////////////// int run() { cout << "Student testing" << endl; strip(); return 0; } Here is the instruction: Write a filter function named strip that removes C++ comments from input, sending the uncommented portion of the program to output. Your program should work with both single line (//) comments, and multi-line (/* */) comments. + A...
Help me with this step-by-step reaction please
Br CH3OH Include a mechanism for the above reaction
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CHEM 2000 Which is biggest: (putting it together) 12. Complete the following synthetic pathway. Include above the arrows the type of process or the reagent or catalyst needed for the transformation. and include the intermediate products between the arrows. OH
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Would someone mind helping me with the following organic
chemistry question.
Please justify/explain your answer. Thank
you!
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QUESTION 21.
Fill in the missing product, reagent, or substrate for each of the
following transformations. Use wedge/dash notation, as appropriate,
to show stereochemistry.
1. 03 2. S(Mei2 - Li 一 COSH Me-CI | Q- AICI: CO2H Two products include stereochemistry): Bry, CCI OH Br + enantiomer
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you guys help me with missing compounds or reagents and show, if
any, stereochemistry. thanks !
+ Brz Intermediate Product t BH₂ THE tha of- + H Br peroxide ho + CH3 - 0 c(CH3)4", t. Gush heat cl Nal Aceton
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Identify the missing reagents, reactants or major products (A - I) required to complete the transformation shown below. Clearly show stereochemistry for all stereo specific reactions.
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that's is all the question is giving me, what is it missing?
[Review Topic (References Use the References to access important values if needed for this question Consider these compounds: A. Cr(OH)3 B. Fe(OH)3 C. Co(OH)2 D. PbBr2 Sred Complete the following statements by entering the letter(s) corresponding to the correct compound(s). (If more than one compound fits the description, include all the relevant compounds by writing your answer as a string of characters without punctuation, c.2,...
Does anyone know the COMPLETE mechanism for this reacrion. Please
help me thank you!