Organic Chemistry

Refer to the 1H NMR spectrum of the 2-aminocyclohexanol and measure the coupling constants for the protons at 2.5 ppm and 3.2 ppm - The protons are adjacent to the NH and OH respectively. Use these coupling constants to provide evidence that the product is structure shown below and explain each proton coupling. This is the trans di-equatorial product. Typical J values are: Jaxial-axial = 8 to 13 Hz Jequatorial - equatorial = 2 to 6 Hz

Lab report - The Kinetics of the Hydrolysis of Ethyl Acetate

5. RESEARCH. Describe the chemical reactivity of your chemical in another context (i.e. other types of reactions it might be involved in, which are not mentioned in this article).

4. For the main chemical, provide the relevant reaction (s) in which it is involved.

Make the physical model and draw the compound on chemagic. Insert pictures below as indicated. Purpose: Observe physical differences between cis/trans isomers and which bonds can rotate and which cannot. Use the physical models to rotate atoms to see if it rotates.

Make the physical model and draw the compound on chemagic. Insert pictures below as indicated. Purpose: Observe physical differences between planar and non-planar portions of the molecule.

Question 51 (0.0001 points) Saved (5 marks) Add bonds (double or triple bonds) and lone pairs to the following incomplete structure where required. Include all formal charges where appropriate. Hand write your answer. Select the tickbox when you have completed the question.

Draw detailed curly arrow mechanism for the reaction below: Me ME CH2 BrCCI3

Q2: Predict what the main product of the following organic reactions?

(6 pts.) 1. Give the major organic product(s) including any appropriate stereochemistry. H₂CO OH OEt OH CH3 CH₂ 1. SOCI ₂. pyr 2. CH₂OH + 3. CH₂CH₂CH₂MgBr (2 eq) 4. H₂0* 1. CH3CH₂CH₂CH₂NH₂, DCC 2. LAH 3. H₂O* 1. LDA, -30°C 2. CHyCH,CH,CH,C + Eto OE! OH¹ EIO ¹ Eto¹