Predict the intermediate 1 and final product 2 of this organic reaction: علامہ CN + H NaOMe H* 1 2 work up You can draw 1 and 2 in any arrangement you like. Note: if either 1 or 2 consists of a pair of enantiomers, just draw one structure using line bonds instead of 3D (dash and wedge) bonds at the chiral center.
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- Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the acetoxy with the para position in phenyl acetate. phenyl acetate ● CH3 • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. In cases where there is more than one answer, just draw one. Sn [F ?Predict the product of this organic reaction: OH CH3-C-CH3 CH3 [0] P + H₂O Specifically, in the drawing area below draw the condensed structure of P. If there isn't any P because this reaction won't happen, check the No reaction box under the drawing area. Note for advanced students: you can assume the reaction is run under mild conditions. Click anywhere to draw the first atom of your structure. X Ö Ś2. Draw structures for the following systems. If more than one isomer is possible, draw strcutures for all the possible isomers. Benzene ring with a methyl group and a nitro group (Draw all possible isomers, and name them) Benzene ring connected to a heptane chain (Draw all possible isomers, and name them) 2-benzyl-3- methylbutan-1-ol
- Draw the product(s) of the following reactions. CH3(CH₂)7-CEC-(CH₂)7-C Y [*** OH • Consider E/Z stereochemistry of alkenes. • If no reaction occurs, draw the organic starting material. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu. H₂C=CH₂ H₂ Lindlar catalyst O $ [ ] كر [References] ChemDoodle Prev2. The molecules shown below are four terpineol isomers. They are isolated from plants and have distinct aromas. For example, a -terpineol is a common perfume ingredient and smells similar to lilacs. Hol H-O- a-terpineol B-terpineol Y-terpineol 4-terpineol A) Draw a structural isomer of terpineol that meet the following criteria. You should draw one unique structure for each set. You must draw each molecule twice, once as a skeletal structure and once as a complete Lewis structure showing all atoms, bonds, and lone pairs of electrons. i. Does not have a ring. ii. Has an E alkene. iii. Has a secondary alcohol. iv. Does not contain an alcohol. B) Draw a complete Lewis structure of a-terpineol showing all bonds, atoms and lone pairs of electrons.Predict the products of this organic reaction: لا IZ H3O+ ? • Draw all the reasonable products in the drawing area below. If there are no products, because no reaction will occur, check the box under the drawing area. • Include both major and minor products, if some of the products will be more common than others. • Be sure to use wedge and dash bonds if you need to distinguish between enantiomers.
- Draw a structural formula for the missing organic product in the reaction below. H₂SO4 + + CH3CH2OH ? H₂O H OH • You do not have to consider stereochemistry. •You do not have to explicitly draw H atoms. CHA ?5A Explain which of the following statements are true and which are false. i. N,N'-dicyclohexylurea (DCU) is the dehydrating reagent that converts a carboxylic acid to the corresponding anhydride. ii. The fact that carbonyl compounds have a lower boiling point than alcohols with the same C atoms is because the molecular dipole moment of carbonyl compounds is less than that of alcohols. iii. 3-Methylbut-2-en-2-ol is the only tautomeric structure of 3- methylbutan-2-one.With the molecular formula C4H8O , I ask you to draw 3 molecules: an aldehyde, a ketone and an enol.For each molecule, you must: a) Complete detailed Lewis structure;b) Make the 3D structure respecting the connection angles;c) Determine which intermolecular interactions are present if you glue 2 twin molecules together (2 aldehydes together, 2 ketones together, 2 enols together, therefore 3 situations to analyze).
- Alcohols undergo an oxidation reaction to yield carbonyl compounds on treatment with CrO3. For example, 2-tert-butylcyclohexanol gives 2-tert-butylcyclohexanone. If axial OH groups are generally more reactive than their equatorial isomers, which do you think reacts faster, the cis isomer of 2-tert-butylcyclohexanol or the trans isomer? Explain.Predict the major products of this organic reaction: OH H 1. LIAIH 2. H₂O ? Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure.Please answer the following pertaining to organic chemistry.