CrO3/H+ it is an oxidizing reagent aldehyde group is react with this reagent they given carboxylic acid product
What is/are the missing reagent(s)in the following reaction? 1)03 2)Zn/H307 CrOz/H Dess-Martin periodinane 1)NaBH4 2)H307 1)LIAIH4...
What is/are the missing reagent(s) (A) in the following reaction? Α CH3CH2——OH 1)LIAIH4 2)H307 1)CN 2)H30+/heat HCOO- CrOz/H 1)NaBH4 2)H30+
Choose the best reagent(s) for carrying out the following conversion from the list provided below. a. 1. e. f. g. CH3MgBr, ether H307 PBr3 NaOH (CH3)3SiC1, (CH3CH2)3N CH3MgBr, ether H30+ LiAlH4, ether 1. p-TosC1, pyridine 2. NaOH CrO3, H2SO4, H2O 1. NaBH4, ethanol 2. H30 Dess-Martin periodinane , CH2Cl2 1. h. 3. d. 1. H30+ HO CH: OH
Chapter 19: More Reactions Name: 1. Complete the following reaction scheme. 1.2 eq. MeMgBr Dess-Martin Periodinane TMSCI Pyridine 2. H₂O* n-BuNF POCIE pyridine H2C-PPh3 2. Synthesize the following compound starting from cyclohexene.
Specify the reagent you would use in each step of the following synthesis: I step 1 step 2 Reagents Available a. LiAIH4 b. H2SO4 c. HCI f. PBrz k. CH2CH2MgBr g. Dess-Martin periodinane (DMP) 1. CH5MgBr (phenylmagnesium bromide) h. NaH m. (CH3)2CHMgBr i. NaOH n. Croz j. CH3MgBr d. HBr e. SOCI2 Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 step 2 Reagents Available a. LIAIHA f. PBr3 b. H2SO4 c. HCI d. HBO e. SOC2 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CH.MgBr (phenylmagnesium bromide) h. Nah m. (CH3)2CHMgBr 1. NaOH n. Croz J. CH3MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 Submit Answer Retry Entire Group 9 more group...
Select the method(s) that would be successful in producing the product starting from the given reactant in good yield. Note: The steps in a method are written in the order carried out. -OH Method I: (a)CrOz/H+,(b)CH2MgBr,(C)H30+,(d)CrOz/H. Method II:(a)PBr3, (b) Mg, (c)CO2, (d)H307, (e)CH2MgBr, (f)H20+. Method III:(a)PBr3, (b)Mg, (C)HCOCH3,(d)H307, (e) CrOz/H. Method IV:(a)Dess-Martin reagent, (b)CH3CHPPh3, (c)03, (d)Zn/H+. O Method III Method 1,111 and IV Method Ill and IV O Method I and III Method IV
What is/are the missing reagent(s) (A) in the following reaction? CH3—CH, —C—OH - CH3-CH2 ——o—chy CH3OCH3 CH3OH/H/heat O H2SO4 CrOz/H+ 1)CN 2)H30+/heat
Question 15 2.5 pts What reagent is missing in the following reaction? CN Reagent CH3MgBr followed by H30+ DIBALH followed by H30* LIAIH4 followed by H2O cat. HCI and H20 Question 16 2.5 pts An unknown compound shows an infrared absorption around 2250 cm (medium intensity). What structural fragment could be causing this absorption? carbonyl O-H nitrile ON-H Previous Next Question 17 2.5 pts Which pair of compounds would be classified as tautomers? . ale Conto ud.& 11 IV Question...
What is/are the missing reagent(s) (A) in the following reaction? None of the choices 1)CH3 CHP(Ph)3 1)CH2CH2Cl/Mg 2)H307 O 1)CH3C1+Cul+ 2Li 2)H30+ 1)CN2)H20+/heat
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 Cl Reagents Available f. PBr3 g. Dess-Martin periodinane (DMP) . C6H5MgBr h. NaH i. NaOH j. CH3MgBr k. CH3CH2MgBr a. LiAIH4 b. H2SO4 c. HCI d. HBr e. Soci2 (phenylmagnesium bromide) m. (CH3)2CHMgBr n. CrO3 Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2