(R)-carvone only exist in cyclic form. Hence we must have to draw the cyclohex-2-en-1-one ring.
The IUPAC name of carvone is: 2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-one.
When we do not use the ring, it will not be (R)-carvone anymore.
The structure is shown below:
How do you draw rhe structure of R-carvone (C10H14O) without using the ring ? (long way)
Draw the structure of the aryldiazonium salt AND the structure
of the activated ring.
Consider the structure of the azo dye called alizaFind thee yellow R (below). Show the reagents you would use to prepare this compound via an azo coupling process.
You react (R)-Carvone with Palladium on Carbon (Pd/C) and heat, to create a transfer-hydrogenation reaction. a) Would the outcome of the reaction be different if you used S-Carvone? Explain your answer. b) In addition to a TLC plate comparing the reactants and products, how do you know a reaction occured?
This question is referring to a glucose ring structure How does ring closure affect structural variability? That is, can the ring form of glucose have as many different structural shapes as the chain form of glucose? Is this 6-member glucose ring actually flat (planar)? Why/why not? Where is the carbonyl group in the glucose ring? Can you convert the ring to the chain without breaking bonds? How many carboxyl groups are in this molecule? How many dissociable groups? Could you...
How to draw a target like this in python without using circle
function??!
How to draw a target like this in python without using circle function??!
WHAT CLASS IS THIS? HOW DO YOU KNOW? WHAT IS THE LONG BLUE STRUCTURE? WHAT DOES IT DO? WHAT PHYLUM IS THIS? HOW DO YOU KNOW?
CH3CH2CH2CH_CH2CH2Cci + CH3CH2OH a. Draw the structure of the tetrahedral intermediate INITIALLY FORMED in the reaction shown. • You do not have to consider stereochemistry. • Do not include counter-ions, e.g., Na", r', in your answer. • In cases where there is more than one answer, just draw one. 2 C- o- / /.000- 1 H, CH b. Draw the structures of the final acyl transfer products obtained. • You do not have to consider stereochemistry. • Draw organic products...
draw a schematic of a two nucleotide long single stranded DNA and indicate the 5' end 3'end. You do not have to draw the structure of the base, innstead you can indicate them as B1 and B2. makr sure you draw the sugar and phosphate explicity with the ring numbering for the sugar.
How do you build a D flip-flop without using decoders and using combinational logics?
A thin ring of radius R and mass M rolls without slipping along a level track. It has an initial linear, or translational velocity (of the center of gravity) of 3.50 m/s. The ring rolls to the end of the track, where the track curves upward. The center of gravity of the ring rises to a maximum height h above its initial level. Note that V is the symbol for the linear, or translational velocity (of the center of gravity)...
organic chem draw the structure
Draw the structure of 3-ethyl-2-methylpentane. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. Z OOO- ChemDoodle