Which of the following is correct? а. When a Grignard reagent reacts with a ketone, the addition product is a primary alcohol When a Grignard reagent reacts with a ketone, the addition product is a secondary alcohol С. When a Grignard reagent reacts with a aldehyde, the addition product is a tertiary alcohol d. None of the above are correct b.

Which of the following is correct? а. When a Grignard reagent reacts with a ketone, the addition product is a primary alcohol When a Grignard reagent reacts with a ketone, the addition product is a secondary alcohol С. When a Grignard reagent reacts with a aldehyde, the addition product is a tertiary alcohol d. None of the above are correct b.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Starting from benzene as the only organic reagent you have and use any other inorganic reagents to prepare:
Convert benzene into attached compound. You may also use any inorganic reagents and organic alcohols having four or fewer carbons. One step of the synthesis must use a Grignard reagent.
Show how to prepare each Gilman reagent from an appropriate alkyl or vinylic halide. Q.Nonane
8) The product of Claisen condensation is a) a-keto ester b) B-keto ester c) 8-keto ester 9) reaction of cyclohexanone with formaldehyde and dimethyl amine in Mannich reaction give- CH3 CH3 CH3 CH3 CH3 b) C) a) CH3 Na OEt ? 10) 2 mole 2-methyl cyclopentanone CH3 CH3 CH3 G. G CH3 CH3 c) b) CH3
Which carbon of indole is easily attacked by an electrophile? 4 5 2 N. В. З С.4 D. 5 ZI
What are the major products obtained when each of the following ethers is heated with one equivalent of HI?
Enols are quite reactive toward electrophiles than alkenes because: а. The OH group has a powerful electron-donating O resonance effect b. A resonance structure can be drawn that places a negative charge on one of the carbon atoms, making this carbon electrophilic С. The enol can react with nucleophilic carbon to form a new bond to carbon d. None of the options are correct
Acetals are often prepared during the synthetic sequence to protect the carbonyl group of an aldehyde or ketone. Such an acetal is not reactive to each of the following reagents except: a.) LiAlH4 b.) PCC(Collins) c.) H3O+ d.) RMgBr e.) NaOH
Which compound will react most rapidly with acetaldehyde? A.propylmagnesium chloride B.cyclopropyl magnesium iodide C.propenylmagnesium bromide D.propynylmagnesium bromide
QV: Starting from Cyclohexanol as the only organic reagent you have and use any other inorganic reagents to prepare:
A compound X with carbonyl groups was reduced using NaBH4 and the product is as shown in the photo. What is the possible structure of the starting compound?