Reagent for step:1: j) CH3MgBt
Reagent for step:2: e) SOCl2
Explanation: Reaction of grignard reagent with ketone produces alcohol as product. Now, reaction of alcohol with SOCl2 produces alkyl halide as product.
Specify the reagent you would use in each step of the following synthesis: step 1 step...
Specify the reagent you would use in each step of the following synthesis: Cl step 1 step 2 Reagents Available a. LiAIH4 f. PBr3 k. CH3CH2MgBr I C6H5MgBr g. pyridinium c. HCI d. HBr e. soci2 chlorochromate (PCC) h. NaH i. NaOH j. CH3MgBr (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
Specify the reagent you would use in each step of the following synthesis: Specify the reagent you would use in each step of the following synthesis: step 1 step 1, step 2 step 2 =cHCH3 Reagents Available a. LiAlH4 b. H2SO4 c. HCI f. PBr3 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CHgMgBr (phenylmagnesium bromide) h. NaH m. (CH3)2CHMgBr i, NaOH n. Cro3 j. CH3MgBr d. HBO e. SOCI2 Write the letters of the reagents in the boxes below....
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...
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
Review Topics] Specify the reagent you would use in each step of the following synthesis References H step 1 step 2 Reagents Available a. LiAIH4 b. H2SO4g. Dess-Martin periodinane (DMP) I. CoHsMgBr c. HC d. HBr f. PBr3 k. CH3CH2MgBr h. NaH i. NaOH j. CH3MgBr (phenylmagnesium bromide) m. (CHa)2CHMgBr n. Cro Write the letters of the reagents in the boxes below Reagent for step 1 Reagent for step 2 Retry Entire Group 9 more group attempts remaining Submlt Answer
help Specify the reagent you would use in each step of the following synthesis: CH3 step 1 step 2 Reagents Available f. PBr3 a. LiAIHA b. H2SO4 c. HCI d. HBO e. SOCI2 g. pyridinium chlorochromate (PCC) h. NaH k. CH3CH2MgBr I. CHgMgBr (phenylmagnesium bromide) m. (CH3)2CHMgBr n. Cro3 1. NaOH 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 No more group attempts...
These synthesis reactions are kicking my butt and I'd appreciate some help with how to go about answering these, or if anyone has any pointers on how to look at these types of problems. Thank you! Specify the reagent you would use in each step of the following synthesis: CH3 H3C CH3 step 1 step 2 H3C CH3 Reagents Available a. LiAIHA b. H2SO4 c. HCI f. PBr3 K. CH3CH2MgBr g. Dess-Martin periodinane (DMP) L. CH MgBr (phenylmagnesium bromide) h....
Specify the reagent you would use in each step of the following synthesis: 1 pts 2rec step 1step 2 1 pts 2req Reagents Available a. LiAIH4 b. H2SO c. HCI d. HBr e. SOCI2 f pts 2rec f. PBr3 k. CH3CH2MgBr g. pyridinium chlorochromate (PCC) h. NaH i. NaOH .CHyMgBr (phenylmagnesium bromide) m. (CH3)2CHMgBr n. CrO 1 pts M 1 pts 2req 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: a. LiAIH_4 b. H_2SO_4 c. HCl d. HBr e.SOCl_2 f. PBr_3 g. Dess-Martin periodinane (DMP) h. NaH i. NaOH j. CH_3MgBr k. CH_3CH_2MgBr l. C_6H_5MgBr (phenylmagnesium bromide) m. (CH_3)_2CHMgBr n. CrO_3 Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2
References) Specify both the alcohol starting material and the reagents you would use in each step in a synthesis of the compound shown. If the synthesis requires only two stepsenter "none" for step 3. Alcohol Starting Materials 1. methanol 2. ethanol 3. 1-propanol 4.2-propanol 5. cyclohexanol Reagents available f. PBry a. LiAlH b. H2SO4 c. HCI d. HBr e. SOCI, CrO3, H, SO, H,O NAH I. CH, MgBr; then H, O* J.CH,CH, MgBr, then H, O k. CHỊ CHỊCH, MgBr,...