grop Help me to find the product Pla Oo. Con portavel to an you label it...
Can someone please help me with this? The directions say to give all 4 products, label which ones are kinetic and which ones are thermo. Also, it says to circle which out of the 4, is most stable. Thank you. roducts which are thermo t kinetic Which is mos 01 a Wole. H-Br
If anyone can help me with this page that would be amazing! (10 pts) 1. Answer the following nomenclature questions. a. Allose is the C-3 epimer of glucose. Draw a-D-allopyranose in its most stable chair conformation. b. Draw ß-D-allopyranose in its least stable chair conformation. c. Draw the zwitterionic Fischer projection of L-phenylalanine d. Draw LDA e. Draw ethyl a-D-ribofuranoside (10 pts) 2. The amino acid histidine has an imidizole ring (shown below), which is able to react with an...
Please help me do these 1. Draw the following bonds and label the electronegativity values of each atom. 2. Label the charge (8* or 8') on each atom in the bond (if they exist) and classify the bond as non-polar covalent, polar covalent or ionic. a) H-CI b) C-H c) NHO d) I-Br c) M-5 e) Mg-S DPH f) P-H vcc g) C-C m) AlH h) Al-H
help with this worksheet please! 1. Determine the radical stability with 1 the most stable and 4 the least stable 2. What is the major product of 2-methylpropane mono-chlorination? Cl2 light 3. Calclate AH for chlorination of methane (DHe for CHa-H is 440 kJ/mol; DH° for Cl-Cl is 243 kJ/mol; DH° for CH3-Cl is 432 kJ/mol; and DH° for H-Cl is 353 kJ/mol 4. Draw structure of the most stable radical formed by hydrogen radical abstraction from 3- methylcyclohexene 5....
Could you help me with this? I replaced the cl with OH to get a product, but I don't know if that was correct. Thank you! OH (f) CI pyridine
I am confused on these 5 problem sets. Could you help me fill it out and explain, please! 1) Circle the most acidic proton in this compound H H H H H H H Fill in the product for each a) NaH b) CH3CH Br a) LDA. b) O c) H+, cold
pleas help 5,6,7,8,9,10 III IV 5. The product of free-radical halogenation reactions is an alkyl halide. The major amount of this halide forms during the second step of propagation. However, you should be aware that one possible termination step also forms alkyl halides. Why does the majority of the alkyl halide product come from the propagation step and not the termination step? A. At any given time during the reaction, the concentration of both the alkyl radical and the halide...
the answers i circled are incorrect. can you give me the correct answers and explain why? For each structure. (1) starany asymmetric carbon atom cture as chilor achiraland (4) label any mes structure (2) label enchan asymmetric carbon as Ros tre cabos ) label the CH3 н H- — Br OH Chiral ₂ CH₂Br oH f Br achiral @ CH Bro 24) Give the solvolysis product expected when each compound is heated in ethanol. 25) Predict the reaction product CHCH...
can you help me explain these especially number 2 Predict the major organic product for each of the following elimination reactions, and indicate 1. whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word "racemic" under any compound that is formed as a racemic mixture. g. Br AgNO3 Нао h. HасСНз KOt-Bu Hас Br t-BuOH ф- Draw all possible E2 products (including...
could you please help me with these questions. thank you so much 20. Which reagent would best serve as the basis for a simple chemical test to distinguish between 0 0 CH3CH2CC2C3 and CH3CH2CH2CCH3 a. NaOI (I in NaOH) b. Br CCL c. CrO,/H SO d. NaHCO,/H20 21. Which proton in the following molecule is the most acidic? A) 1 B) 2 C) 3 D) 4 E) 5 22. What product is formed in the aldol reaction of propanal? a....