Build the following molecule: 1-chloroethanol, CH3CHClOH Draw the structure here. Note: recall that when naming alkanes...
Build the following molecule: 1-chloroethanol, CH3CHClOH
Draw the structure here. Note: recall that when naming alkanes it
can numbered from either end of the molecule to give the functional
group the lowest number, so C#1 is the highlighted C and it will
have 4 groups, a CH3, an H, a Cl and an OH group on it. Use wedges
and dashes. Do not cut and paste from the internet, you must show
all 4 groups.
Homework Answers
Add Answer to:
Build the following molecule: 1-chloroethanol, CH3CHClOH
Draw the structure here. Note: recall that when naming alkanes...
Key concepts: molecular represenations, stereolsomers, RS enantiomeric excess, IPAC naming covention Provide the IUPAC name for...
Key concepts: molecular represenations, stereolsomers, RS enantiomeric excess, IPAC naming covention Provide the IUPAC name for each of the following molecules 0% HJC BM How similar are the names for B and C, even though there is the single change to the structure 2 Rank the priorities of these functional groups and substituents using Cahn-Ingold-Prelog nomenclature. Highest priority will be 1 and lowest will be 5; show your rationale CH:CH:CH CH CHCH:CH CHs,-SCH,-CH: CH:CH:CHCH CHCH, -CH2NHOH,-CH:NO Draw dash/wedge representations for...
1. (2 points) Provide the IUPAC name for the following structure. он 2. (2 points) Draw...
1. (2 points) Provide the IUPAC name for the following structure. он 2. (2 points) Draw the structure from the provided name: 5-chloro-2,2-dimethylcyclohexane-1,3-dione. 3. (6 points) The following reaction produces five different substitution and elimination products, (a) Draw these products and (b) rank the stability of the elimination products by using the labels (E1-E3) according to the products as you have entered them. substitution product S1 substitution product S2 HzC04 CF, H-OH elimination product E1 elimination product E2 elimination product...
Chapters 21 and 22 1. Consider the structure shown on the right and answer the following question...
please help with questions!
Chapters 21 and 22 1. Consider the structure shown on the right and answer the following questions about it (fill in blanks or circle proper choice). f4 tl a. Its molecular formula is CH,O 似 and so it fits the general formula for a carbohiydrate, which is C(O b. Specifically, this structure is (a D) an L.) (aldojketo) (pent/hex (ase/ c. Will it be optically active? s d. If the top carbon was converted to a...
Chapters 21 and 22: 1. Consider the structure shown on the right and answer the following questio...
Chapters 21 and 22: 1. Consider the structure shown on the right and answer the following questions about it (ill in blanks or cirele proper choice) (4 a. Its molecular formula is G ,H( )0( , and so it fits the CHOH , general formula for a carbohydrate, which is b. Specifically, this structure is (a D/ an L) (aldo/keto) (pent/hex) (aselose) c. Will it be optically active? d. If the top carbon was converted to a CH,OH, would it...
1. In the H NMR, draw the structure of the molecule directly on the spectrum and...
1. In the H NMR, draw the structure of the molecule directly on
the spectrum and identify each unique proton. Indicate which proton
is responsible for each peak.
2. In the IR spectrum, indicate which functional group is
responsible for each important peak. Attempt to identify at least
five important peaks. In you discussion, indicate which peaks are
most helpful in determining whether or not you converted the
starting material to the desired product.
3. Compare the IR spectrum of...
2-methylocta-4,6-dien-1-amine Assignment 1: Draw your molecule from IUPAC name
2-methylocta-4,6-dien-1-amineAssignment 1: Draw your molecule from IUPAC
name Using the given IUPAC name, draw your molecule Complete the cover page (p.1) of your portfolio with the
following:o Structural formula of the moleculeo IUPAC name Use a thin, clear binder or report cover to protect the
portfolio Submit the following in the binder:o Cover page as described above (page 1)Assignment 2: Formula, Molar Mass and Functional
Groups On a page titled Expanded Structural Formula draw the expanded
structure of themolecule.o Show...
6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8....
6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8. Label the indicated atoms in the structure below as 1º, 2º, 3º, or 4º. PB A A B co 9. Draw Newman projections for the day-diethylane about the C4CS bond, Circle the most stable conforme if you need additional space, please feel free to the backside of this paper 10. Draw the chair conformation and ring-flip for the given compound. Calculate the sterie strain...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the bonding preferences of each atom when you lay out the skeleton of this molecule!) 1. CC Determine the geometry at each "central atom" (a) Does this molecule have any polar bonds? Is the entire molecule polar? (b) What will be the dominant intermolecular force in a sample of this compound? (c) (c) If you had 100.0 g of this compound, how many moles would...
____ 1. The diagram below represents serine, a polar, uncharged amino acid. Which functional group gives...
____ 1. The diagram below represents serine, a polar, uncharged
amino acid. Which functional group gives serine its
distinct property?
a. H3
b. CH2OH
c. –H
d. COO–
____ 2. The monomers shown below are monomers for which of the
following natural polymers?
a. polysaccharides
b. plastics
c. DNA
d. proteins
____ 3. Which of the following processes illustrates the production
of a protein?
a. specific code for amino acids --> amino acid chain -->
gene --> DNA --> specific...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23,...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
Key concepts: molecular represenations, stereolsomers, RS enantiomeric excess, IPAC naming covention Provide the IUPAC name for each of the following molecules 0% HJC BM How similar are the names for B and C, even though there is the single change to the structure 2 Rank the priorities of these functional groups and substituents using Cahn-Ingold-Prelog nomenclature. Highest priority will be 1 and lowest will be 5; show your rationale CH:CH:CH CH CHCH:CH CHs,-SCH,-CH: CH:CH:CHCH CHCH, -CH2NHOH,-CH:NO Draw dash/wedge representations for...
1. (2 points) Provide the IUPAC name for the following structure. он 2. (2 points) Draw the structure from the provided name: 5-chloro-2,2-dimethylcyclohexane-1,3-dione. 3. (6 points) The following reaction produces five different substitution and elimination products, (a) Draw these products and (b) rank the stability of the elimination products by using the labels (E1-E3) according to the products as you have entered them. substitution product S1 substitution product S2 HzC04 CF, H-OH elimination product E1 elimination product E2 elimination product...
please help with questions!
Chapters 21 and 22 1. Consider the structure shown on the right and answer the following questions about it (fill in blanks or circle proper choice). f4 tl a. Its molecular formula is CH,O 似 and so it fits the general formula for a carbohiydrate, which is C(O b. Specifically, this structure is (a D) an L.) (aldojketo) (pent/hex (ase/ c. Will it be optically active? s d. If the top carbon was converted to a...
Chapters 21 and 22: 1. Consider the structure shown on the right and answer the following questions about it (ill in blanks or cirele proper choice) (4 a. Its molecular formula is G ,H( )0( , and so it fits the CHOH , general formula for a carbohydrate, which is b. Specifically, this structure is (a D/ an L) (aldo/keto) (pent/hex) (aselose) c. Will it be optically active? d. If the top carbon was converted to a CH,OH, would it...
1. In the H NMR, draw the structure of the molecule directly on
the spectrum and identify each unique proton. Indicate which proton
is responsible for each peak.
2. In the IR spectrum, indicate which functional group is
responsible for each important peak. Attempt to identify at least
five important peaks. In you discussion, indicate which peaks are
most helpful in determining whether or not you converted the
starting material to the desired product.
3. Compare the IR spectrum of...
2-methylocta-4,6-dien-1-amineAssignment 1: Draw your molecule from IUPAC
name Using the given IUPAC name, draw your molecule Complete the cover page (p.1) of your portfolio with the
following:o Structural formula of the moleculeo IUPAC name Use a thin, clear binder or report cover to protect the
portfolio Submit the following in the binder:o Cover page as described above (page 1)Assignment 2: Formula, Molar Mass and Functional
Groups On a page titled Expanded Structural Formula draw the expanded
structure of themolecule.o Show...
6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8. Label the indicated atoms in the structure below as 1º, 2º, 3º, or 4º. PB A A B co 9. Draw Newman projections for the day-diethylane about the C4CS bond, Circle the most stable conforme if you need additional space, please feel free to the backside of this paper 10. Draw the chair conformation and ring-flip for the given compound. Calculate the sterie strain...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the bonding preferences of each atom when you lay out the skeleton of this molecule!) 1. CC Determine the geometry at each "central atom" (a) Does this molecule have any polar bonds? Is the entire molecule polar? (b) What will be the dominant intermolecular force in a sample of this compound? (c) (c) If you had 100.0 g of this compound, how many moles would...
____ 1. The diagram below represents serine, a polar, uncharged
amino acid. Which functional group gives serine its
distinct property?
a. H3
b. CH2OH
c. –H
d. COO–
____ 2. The monomers shown below are monomers for which of the
following natural polymers?
a. polysaccharides
b. plastics
c. DNA
d. proteins
____ 3. Which of the following processes illustrates the production
of a protein?
a. specific code for amino acids --> amino acid chain -->
gene --> DNA --> specific...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
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