Can you explain how to approach this problem and then the steps you use to get...
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.
(2) Predict the major product(s) for each of the following reactions. Be sure to indicate stereochemistry and draw enantiomers when appropriate. Clearly show stereochemistry with two lines in the plane and a wedge and/or dash at the chirality center(s) No reaction mechanisms are necessary C3 C3
Can you show how to approach and solve this problem to get the
answer in this picture.
6.3-10. The cantilever shaft shown in the figure is subjected to distributed torsional moment t(x) = to 11-G)21. r12 Find the reaction torque at A, and then plot the TMD. Answer 2Lto 2Lto Problem 6.3-10 t(x)
can you please explain each step and why its occurring!!
can you explain why each step is occuring as well. please! 3. Show how the following conversions could be carried out in three or fewer steps. Provide structures for each intermediate, which would be isolated and indicate reagents and conditions for each step. Pay close attention to stereochemistry. CH3 ...CH • ? for • 208 OCH2CH3
Please explain the steps needed and how to
approach the problem
aler len celsosl
1. (4 pts) Convert the following condensed structural formulas into skeletal (line angle) structures a) CH3CH2CH(OH)CHCHCH: b) NH2CH=CCCH2CHO 2. (8 pts) An ion with the structural formula (CH CHOJ can be represented with two different resonance structures. a) Draw the two resonance structures below and circle the major contributing structure. b) Specify the hybridization of each carbon atom.
Can
someone tell me if these structures are correct? can you please
write the correct structures as well. i am also have a bit of
trouble with questions 4-6. please help thank you.
3- Draw the structural formulas for the following compounds: a))2,2,5,5-tetramethylheptane C H3 b) 6,6,6-trichloro-1-hexyne ) 3-chloropropanal Cy Hi CO d) trans-2.2,5,5-tetramethyl-3-hexene CH c l e) 3-methyltoluene 3-bromo-5-methylphenol CaH2rO F10 F9 4- Complete the following reactions a) b) Br c) [Ol HaC он HO CH3 5- A student...
Can you explain how to get this answer? I’m confused on how to
get this specific lewis structure from the information given and
where the C2H4 would go in the final product
The following addition reaction will proceed when bromine forms two radicals via homolytic cleavage. The radicals then react with ethene to form which product? HH C= C + 1 H Bra , Br
If i could get some help on either of these 2 worksheets i
would greatly appreciate it! Thanks so mich!
do some molecules with the same formula (or even connectivity!) have different properties? ACQUIRE (USING MODELS!) 1. Fill in the following tables and BUILD each structure as you go. Have your instructor check your answers after each table or as directed Name and Condensed structure Skeletal structure Molecular formula Name: C8H18 2,3-dimethylhexane Molecular formula: C&HI8 Constitutional (structural) isomer of A...
If you could please explain how to get these answers,
thankyou.
Problem 3: Predict the products of these reactions (a) H(b) Cr(CO)6 + OH (c) Problem 4: Predict the products of these reactions NO I PR R3P PR3
please explain the steps to get to the answer
Find AH° for the reaction: 2 C,H,OH (1) + 0, (g) → 2 CH CHO (g) + 2 H,0 (9) GIVEN: C,H,OH (1) + 3 0, (g) → 2 CO, (g) + 3 H,0 (9) AH° = -1236 kJ 2 CHỊCHO (g) + 5 0, (g) + 4CO, (g) + 4 H,O (g) AH = -2207 kJ 2 CH OH (1) + 6 0, () — 4 CO, (g) + 6...