A. Alcohol to alkyl halide ---》 1)SOCl2,DMF,dichloro methane, 0-5°C. OR PCl3/PCl5,dichloro methane.
B. Alkyne to ketone using H2O,H2SO4,HgSO4 the enolate form in the reaction which gives two products.
C. Ester to alcohol --------》 1) 2*CH3CH2.Mg.Br , Ether,0-5°C
D. Alcohol to ether ----------》1) H2SO4,H+ OR 1) strong base KOH or NaOH.to form alcoxide 2) Ph-CHBr-CH3, THF,0-5°C.
E. Alkyne to cis alkene ------》1) Lindlars catalyst,H2 gas pressure.
F. Primary alcohol to aldehyde -----------》 Its a oxidation reaction of alcohol. CrO3 or pyridinium chloro chromate PCC,FMF
G.Baeyers reagent condition,Alkaline KMnO4,[O],H-OH at 298K temp. Which oxidised the alkyne to resp.keron and carboxylic acid.
say for each to 2. (21 p ) Provide the reagents, solvents, and the reaction transformation...
Provide all reagents and solvents needed to complete
transformation.
Provide all reagents and solvents needed to complete transformation. (E)-2-choro-7-methyloctane rightarrow trans 2 octene Cannot use any reagents with aldehyde or alkene). (S) - 2 - iodo - 4 - methylhexane rightarrow (R)-4-methylhexyne rightarrow 2 - bromopropene - (2R 3R) - 2 - chloro - 3 heptanol (- OH group on 3rd carbon) (1R 2R) - 1 - chloro - 2 methylcyclopentane rightarrow (Z) - 2 - bromo - 2 -...
1. Provide the necessary reaction conditions (reagents
and solvents) to perform the indicated transformation. More than
one step may be necessary. Synthesis of reagents used in the
transformation are not required. Consider equivalents, selectivity,
and stereochemistry. Very little partial credit will be
given.
مل مل . . است Me OH CH سرعت -- له Me Me OH Me H0 Me Me- DH - We Me لكم OH 0 م --کمت و سلم . یک ما لكم . Me Me Me
Provide the reagents, solvents, and reaction
conditions for each of the transformations shown.
Question 4: он Br Step 1 Step 2 Step 3 、
2. Given both reactants and products, provide correct chemical
reagents and solvents to complete the reaction. You might have
multiple choices:
2. Given both reactants and products, provide correct chemical reagents and solvents to complete the reaction. You might have multiple choices: a. (i) + enantiomer OH do — Jaco Y -CHO CHO
1) Provide the missing reagents to complete each
transformation. (Need to use correct reagents in CORRECT
order)
3. (20pts) Provide the missing reagents needed to complete each transformation below. Each arrow represents a single reaction. Do not exceed the number or reactions allowed for each transformation. You will have to use the correct combination of reagents in the correct order to receive full credit. (4pts for correct reagents and correct order for each transformation a-e)
2. Given both reactants and products, provide correct chemical reagents and solvents to complete the reaction. You might have multiple choices: 3. Propose a plausible synthesis for each of the following transformations: od
each transformation shown below requires at least two steps.
provide the reagents/conditions for each transformation.
5. Each transformation shown below requires at least two steps. Provide the reagents/conditions for each transformation. (20 pt A:Br2, Febra Bich - CH Reagents ? Reagents A-? CHNO₂, H₂SO4 2.) Fe, HCl 3.) NaOH Reagents D- Reagents ? Reagents ? 6. Predict the product from the Birch reduction shown below: (3 pts) Na, NH3 CHLOH
For each numbered transformation provide the reagents which would best achieve the reaction shown in the corresponding blank below. (1 ) The appropriate work-up is assumed for each transformation. Coc, albas -12 17 15 L. 13 cod 8. SCH, OH - CH
5. Provide the complete reaction conditions (reagents, solvents) required transformations. More than one step may be required for each reaction arrow, be numbered 1), 2) etc. (12 marks) ents, solvents) required to complete the following uired for each reaction arrow, in which case the steps must DO
Each transformation shown below requires at least two steps. Provide the reagents/conditions for each transformation. CHS Reagents F-? Reagents A=? CH Reagents D=? Reagents B=? CH Recents C-