For this reaction: 1. xs NaNH2 2. H2O Br Br Two sets of reagents are necessary...
Select the best reagents for the reaction below.
Select one:
1. OsO4; 2. NaHSO3, H2O
NaNH2
H2, Pt
Na, NH3(l)
H2, Lindlar’s catalyst
Select the best reagents for the reaction below.
Select one:
NaNH2
1. O3; 2. H2O
KMnO4
1. BH3·THF; 2. H2O2, NaOH
H2SO4, H2O
os o
The below reaction is accomplished with one reagent. Br The letters below represent all reagents you have learned in chapters 6-8. Which of the below reagents would you use to accomplish this process? Enter the ONE correct letter below. • a. H2SO4, H20 b.HBO c. Br2 • d. Br2. H20 e. 1) BH3 (or R2BH), 2) NaOH, H20 • f. 1) OsO4, 2) NaHSO3, H20 g. 1) O3. 2) CH3SCH3 h.mCPBA • i.H2.Pd/C j. NaNH2 k 2 eg NaNH2 ....
4.(18 points) Using the arrow, provide the detailed reaction conditions necessary to give the following. You do not need to provide any starting material or product, just the reaction conditions (see example below) 1.B Example: Show reagent 'B' followed by aqueous acid: 2. H30 a. Markovnikov addition of H2O to a double bond: b. Anti-Markovnikov addition of H2O to a double bond: c. Markovnikov addition to form an alkyl bromide from an alkene: d. Reaction conditions to change 1,2-dimethylcyclohexene into...
5) Provide the product of each reaction shown below NaOH H2O 1) NaCN Br 31H0 2) CH3CH2MgBr 3) H20 COH 1) SOCI 2/(CH3CH2)2NH Bra CH3COOH 1) NaOEU/EVOH + HC0 Et 2) H30* ♡ weak + . CHOCOCH,en CHOCOCH CN base
Use retrosynthetic analysis to design a synthesis on paper for the transformation of 2-chloro-3-methylbutane into 3-methylbutanal as shown below. You'll need six of the following reagents. Order the correct ones in order 1-6.The one you don't use will be number 7 through 10. But order the 7+ ones in analagous order to the synthesis. For instance, if your first step is a zaistev elimination, and you have a bulky base and a nonbulky base, then reagent number 7 should be the bulky base. If your...
1-24 need help really lost
Proton Transfer: deprotonation D. 1) Add the appropriate curved arrows for the following deprotonation step. Also add the other product notice how the Tema s can be converted to this by use of a strong base such as sodium a sodium ion (Na) is not drawn, in this case it is just a spectatorio PCW27 - Mechanistic steps - Part Name: Time spent 2) Label the above compounds with the appropriate name from the previous...
Questions 2-10 please!!
1) A substitution reaction is: [2] a) A reaction during which an OH group of a molecule is replaced by a halogen. b) A reaction during which water is the leaving group. c) A reaction during which a functional group of a molecule is replaced by an electrophile. d) A reaction during which a functional group of a molecule is replaced by another functional group. V 12 2) Substitution reactions are classified either as electrophilic or nucleophilic...
i need help with the postlab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....